Linked Data
ClinVar Variation Id:
127287
dbSNP Id:
rs587779789
gnomAD v2:
5-112174659-A-C
gnomAD v3:
5-112838962-A-C
gnomAD v4:
5-112838962-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838962A>C , CM000667.2:g.112838962A>C | GRCh38 |
| NC_000005.9:g.112174659A>C , CM000667.1:g.112174659A>C | GRCh37 |
| NC_000005.8:g.112202558A>C | NCBI36 |
| NG_008481.4:g.151442A>C , LRG_130:g.151442A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.3033A>C | ENSP00000484935.2:n.3033A>C | |
| ENST00000504915.3:c.3422A>C | ENSP00000473355.2:p.Gln1141Pro | |
| ENST00000505350.2:c.*3374A>C | ENSP00000481752.1:n.*3374A>C | |
| ENST00000507379.6:c.3314A>C | ENSP00000423224.2:p.Gln1105Pro | |
| ENST00000509732.6:c.3368A>C | ENSP00000426541.2:p.Gln1123Pro | |
| ENST00000512211.7:c.3368A>C | ENSP00000423828.3:p.Gln1123Pro | |
| ENST00000257430.9:c.3368A>C MANE Select | ENSP00000257430.4:p.Gln1123Pro | |
| ENST00000257430.8:c.3368A>C | ENSP00000257430.4:p.Gln1123Pro | |
| ENST00000502371.2:c.1721A>C | ||
| ENST00000507379.5:c.3314A>C | ENSP00000423224.1:p.Gln1105Pro | |
| ENST00000508376.6:c.3368A>C | ENSP00000427089.2:p.Gln1123Pro | |
| ENST00000508624.5:c.*2690A>C | ENSP00000424265.1:n.*2690A>C | |
| ENST00000512211.6:c.3368A>C | ENSP00000423828.2:p.Gln1123Pro | |
| ENST00000520401.1:c.230+9990A>C | ||
| NM_000038.5:c.3368A>C | NP_000029.2:p.Gln1123Pro | |
| NM_001127510.2:c.3368A>C | NP_001120982.1:p.Gln1123Pro | |
| NM_001127511.2:c.3314A>C | NP_001120983.2:p.Gln1105Pro | |
| NM_001354895.1:c.3368A>C | NP_001341824.1:p.Gln1123Pro | |
| NM_001354896.1:c.3422A>C | NP_001341825.1:p.Gln1141Pro | |
| NM_001354897.1:c.3398A>C | NP_001341826.1:p.Gln1133Pro | |
| NM_001354898.1:c.3293A>C | NP_001341827.1:p.Gln1098Pro | |
| NM_001354899.1:c.3284A>C | NP_001341828.1:p.Gln1095Pro | |
| NM_001354900.1:c.3245A>C | NP_001341829.1:p.Gln1082Pro | |
| NM_001354901.1:c.3191A>C | NP_001341830.1:p.Gln1064Pro | |
| NM_001354902.1:c.3095A>C | NP_001341831.1:p.Gln1032Pro | |
| NM_001354903.1:c.3065A>C | NP_001341832.1:p.Gln1022Pro | |
| NM_001354904.1:c.2990A>C | NP_001341833.1:p.Gln997Pro | |
| NM_001354905.1:c.2888A>C | NP_001341834.1:p.Gln963Pro | |
| NM_001354906.1:c.2519A>C | NP_001341835.1:p.Gln840Pro | |
| NM_000038.6:c.3368A>C MANE Select | NP_000029.2:p.Gln1123Pro | |
| NM_001127510.3:c.3368A>C | NP_001120982.1:p.Gln1123Pro | |
| NM_001127511.3:c.3314A>C | NP_001120983.2:p.Gln1105Pro | |
| NM_001354895.2:c.3368A>C | NP_001341824.1:p.Gln1123Pro | |
| NM_001354896.2:c.3422A>C | NP_001341825.1:p.Gln1141Pro | |
| NM_001354897.2:c.3398A>C | NP_001341826.1:p.Gln1133Pro | |
| NM_001354898.2:c.3293A>C | NP_001341827.1:p.Gln1098Pro | |
| NM_001354899.2:c.3284A>C | NP_001341828.1:p.Gln1095Pro | |
| NM_001354900.2:c.3245A>C | NP_001341829.1:p.Gln1082Pro | |
| NM_001354901.2:c.3191A>C | NP_001341830.1:p.Gln1064Pro | |
| NM_001354902.2:c.3095A>C | NP_001341831.1:p.Gln1032Pro | |
| NM_001354903.2:c.3065A>C | NP_001341832.1:p.Gln1022Pro | |
| NM_001354904.2:c.2990A>C | NP_001341833.1:p.Gln997Pro | |
| NM_001354905.2:c.2888A>C | NP_001341834.1:p.Gln963Pro | |
| NM_001354906.2:c.2519A>C | NP_001341835.1:p.Gln840Pro |