WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
Linked Data
gnomAD v4:
2-151497630-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.151497630C>A , CM000664.2:g.151497630C>A | GRCh38 |
| NC_000002.11:g.152354144C>A , CM000664.1:g.152354144C>A | GRCh37 |
| NC_000002.10:g.152062390C>A | NCBI36 |
| NG_009382.2:g.241858G>T , LRG_202:g.241858G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000434685.6:c.3075-5136G>T (NEB) | ||
| ENST00000688578.1:c.900-597G>T (NEB) | ||
| ENST00000690043.1:c.6378-3377G>T (NEB) | ||
| ENST00000693000.1:n.2657-5136G>T (NEB) | ||
| ENST00000397345.8:c.24296G>T (NEB) MANE Select | ENSP00000380505.3:p.Ser8099Ile | |
| ENST00000427231.7:c.24296G>T (NEB) MANE Plus Clinical | ENSP00000416578.2:p.Ser8099Ile | |
| ENST00000172853.14:c.18826-1262G>T (NEB) | ENSP00000172853.10:n.18826-1262G>T | |
| ENST00000397337.6:c.697G>T (NEB) | ||
| ENST00000397345.7:c.24296G>T (NEB) | ENSP00000380505.3:p.Ser8099Ile | |
| ENST00000409198.5:c.18826-1262G>T (NEB) | ENSP00000386259.1:n.18826-1262G>T | |
| ENST00000413693.5:c.8026-1262G>T (NEB) | ENSP00000410961.1:n.8026-1262G>T | |
| ENST00000421461.6:c.732G>T (NEB) | ||
| ENST00000424585.1:c.610-597G>T (NEB) | ENSP00000404876.1:n.610-597G>T | |
| ENST00000427231.6:c.24296G>T (NEB) | ENSP00000416578.2:p.Ser8099Ile | |
| ENST00000434685.5:c.1395-3377G>T (NEB) | ||
| ENST00000454583.6:c.2754-1715C>A (RIF1) | ||
| ENST00000457745.1:n.579-156C>A (RIF1) | ||
| ENST00000484077.1:n.353-156C>A (RIF1) | ||
| ENST00000498015.2:n.226-5136G>T (NEB) | ||
| ENST00000603639.5:c.24296G>T (NEB) | ENSP00000473894.1:p.Ser8099Ile | |
| ENST00000604864.5:c.24296G>T (NEB) | ENSP00000474498.1:p.Ser8099Ile | |
| ENST00000618972.4:c.24401G>T (NEB) | ENSP00000484342.1:p.Ser8134Ile | |
| NM_001164507.1:c.24296G>T (NEB) | NP_001157979.1:p.Ser8099Ile | |
| NM_001164508.1:c.24296G>T (NEB) | NP_001157980.1:p.Ser8099Ile | |
| NM_001271208.1:c.24401G>T , LRG_202t1:c.24401G>T (NEB) | NP_001258137.1:p.Ser8134Ile | |
| NM_004543.4:c.18826-1262G>T (NEB) | NP_004534.2:n.18826-1262G>T | |
| XM_005246590.1:c.24203G>T (NEB) | XP_005246647.1:p.Ser8068Ile | |
| XM_005246591.1:c.24203G>T (NEB) | XP_005246648.1:p.Ser8068Ile | |
| XM_005246592.1:c.24296G>T (NEB) | XP_005246649.1:p.Ser8099Ile | |
| XM_005246593.1:c.24296G>T (NEB) | XP_005246650.1:p.Ser8099Ile | |
| XM_005246594.1:c.24203G>T (NEB) | XP_005246651.1:p.Ser8068Ile | |
| XM_005246595.1:c.24203G>T (NEB) | XP_005246652.1:p.Ser8068Ile | |
| XM_005246596.1:c.24110G>T (NEB) | XP_005246653.1:p.Ser8037Ile | |
| XM_005246597.1:c.24296G>T (NEB) | XP_005246654.1:p.Ser8099Ile | |
| XM_005246598.1:c.24296G>T (NEB) | XP_005246655.1:p.Ser8099Ile | |
| XM_005246599.1:c.24017G>T (NEB) | XP_005246656.1:p.Ser8006Ile | |
| XM_005246600.1:c.24017G>T (NEB) | XP_005246657.1:p.Ser8006Ile | |
| XM_005246601.1:c.23929-597G>T (NEB) | XP_005246658.1:n.23929-597G>T | |
| XM_005246602.1:c.23924G>T (NEB) | XP_005246659.1:p.Ser7975Ile | |
| XM_005246603.1:c.23929-1262G>T (NEB) | XP_005246660.1:n.23929-1262G>T | |
| XM_005246604.1:c.23929-597G>T (NEB) | XP_005246661.1:n.23929-597G>T | |
| XM_005246606.1:c.23924G>T (NEB) | XP_005246663.1:p.Ser7975Ile | |
| XM_005246608.1:c.23929-3377G>T (NEB) | XP_005246665.1:n.23929-3377G>T | |
| XM_005246610.1:c.23836-3377G>T (NEB) | XP_005246667.1:n.23836-3377G>T | |
| XM_005246611.1:c.24021+3761G>T (NEB) | XP_005246668.1:n.24021+3761G>T | |
| XM_005246612.1:c.23567G>T (NEB) | XP_005246669.1:p.Ser7856Ile | |
| XM_005246613.1:c.23567G>T (NEB) | XP_005246670.1:p.Ser7856Ile | |
| XM_005246615.1:c.23924G>T (NEB) | XP_005246672.1:p.Ser7975Ile | |
| XM_005246616.1:c.*594G>T (NEB) | XP_005246673.1:n.*594G>T | |
| XM_005246617.1:c.21380G>T (NEB) | XP_005246674.1:p.Ser7127Ile | |
| XM_006712541.1:c.23929-1262G>T (NEB) | XP_006712604.1:n.23929-1262G>T | |
| XM_006712542.1:c.24017G>T (NEB) | XP_006712605.1:p.Ser8006Ile | |
| XM_011511224.1:c.24203G>T (NEB) | XP_011509526.1:p.Ser8068Ile | |
| XM_011511225.1:c.23743-3377G>T (NEB) | XP_011509527.1:n.23743-3377G>T | |
| XM_011511226.1:c.22109G>T (NEB) | XP_011509528.1:p.Ser7370Ile | |
| XM_011511227.1:c.19922G>T (NEB) | XP_011509529.1:p.Ser6641Ile | |
| XR_922955.1:n.7838+14295C>A (RIF1) | ||
| XR_922956.1:n.7937-156C>A (RIF1) | ||
| XR_922957.1:n.7839-156C>A (RIF1) | ||
| XM_005246590.2:c.24203G>T (NEB) | XP_005246647.1:p.Ser8068Ile | |
| XM_005246591.2:c.24203G>T (NEB) | XP_005246648.1:p.Ser8068Ile | |
| XM_005246592.2:c.24296G>T (NEB) | XP_005246649.1:p.Ser8099Ile | |
| XM_005246593.2:c.24296G>T (NEB) | XP_005246650.1:p.Ser8099Ile | |
| XM_005246594.2:c.24203G>T (NEB) | XP_005246651.1:p.Ser8068Ile | |
| XM_005246596.2:c.24110G>T (NEB) | XP_005246653.1:p.Ser8037Ile | |
| XM_005246597.2:c.24296G>T (NEB) | XP_005246654.1:p.Ser8099Ile | |
| XM_005246598.2:c.24296G>T (NEB) | XP_005246655.1:p.Ser8099Ile | |
| XM_005246599.2:c.24017G>T (NEB) | XP_005246656.1:p.Ser8006Ile | |
| XM_005246601.2:c.23929-597G>T (NEB) | XP_005246658.1:n.23929-597G>T | |
| XM_005246602.2:c.23924G>T (NEB) | XP_005246659.1:p.Ser7975Ile | |
| XM_005246603.2:c.23929-1262G>T (NEB) | XP_005246660.1:n.23929-1262G>T | |
| XM_005246604.2:c.23929-597G>T (NEB) | XP_005246661.1:n.23929-597G>T | |
| XM_005246606.2:c.23924G>T (NEB) | XP_005246663.1:p.Ser7975Ile | |
| XM_005246608.2:c.23929-3377G>T (NEB) | XP_005246665.1:n.23929-3377G>T | |
| XM_005246610.2:c.23836-3377G>T (NEB) | XP_005246667.1:n.23836-3377G>T | |
| XM_005246611.2:c.24021+3761G>T (NEB) | XP_005246668.1:n.24021+3761G>T | |
| XM_005246612.2:c.23567G>T (NEB) | XP_005246669.1:p.Ser7856Ile | |
| XM_005246613.2:c.23567G>T (NEB) | XP_005246670.1:p.Ser7856Ile | |
| XM_005246615.2:c.23924G>T (NEB) | XP_005246672.1:p.Ser7975Ile | |
| XM_005246617.2:c.21380G>T (NEB) | XP_005246674.1:p.Ser7127Ile | |
| XM_006712541.2:c.23929-1262G>T (NEB) | XP_006712604.1:n.23929-1262G>T | |
| XM_006712542.2:c.24017G>T (NEB) | XP_006712605.1:p.Ser8006Ile | |
| XM_011511225.2:c.23743-3377G>T (NEB) | XP_011509527.1:n.23743-3377G>T | |
| XM_011511226.2:c.22109G>T (NEB) | XP_011509528.1:p.Ser7370Ile | |
| XM_011511227.2:c.19922G>T (NEB) | XP_011509529.1:p.Ser6641Ile | |
| XM_017004177.1:c.24185G>T (NEB) | XP_016859666.1:p.Ser8062Ile | |
| XM_017004178.1:c.24110G>T (NEB) | XP_016859667.1:p.Ser8037Ile | |
| XM_017004179.1:c.23836-597G>T (NEB) | XP_016859668.1:n.23836-597G>T | |
| XM_017004180.1:c.23831G>T (NEB) | XP_016859669.1:p.Ser7944Ile | |
| XM_017004181.1:c.23836-1262G>T (NEB) | XP_016859670.1:n.23836-1262G>T | |
| XM_017004182.1:c.23836-1262G>T (NEB) | XP_016859671.1:n.23836-1262G>T | |
| XM_017004183.1:c.23836-3377G>T (NEB) | XP_016859672.1:n.23836-3377G>T | |
| XM_017004184.1:c.23836-1262G>T (NEB) | XP_016859673.1:n.23836-1262G>T | |
| XM_017004185.1:c.23743-5136G>T (NEB) | XP_016859674.1:n.23743-5136G>T | |
| XR_001738811.2:n.8312-156C>A (RIF1) | ||
| XR_001738812.2:n.8312-1775C>A (RIF1) | ||
| XR_001738813.2:n.8214-156C>A (RIF1) | ||
| XR_001738814.2:n.8214-1775C>A (RIF1) | ||
| XR_001738815.2:n.8214-5404C>A (RIF1) | ||
| XR_001738816.2:n.8214-8580C>A (RIF1) | ||
| XR_001738817.2:n.8213+14295C>A (RIF1) | ||
| NM_001271208.2:c.24401G>T (NEB) | NP_001258137.2:p.Ser8134Ile | |
| NM_004543.5:c.18826-1262G>T (NEB) | NP_004534.3:n.18826-1262G>T | |
| NM_001164507.2:c.24296G>T (NEB) MANE Plus Clinical | NP_001157979.2:p.Ser8099Ile | |
| NM_001164508.2:c.24296G>T (NEB) MANE Select | NP_001157980.2:p.Ser8099Ile |