UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
dbSNP Id:
rs1400545150
gnomAD v2:
4-176661993-AAAGGCATTTTT-A
gnomAD v3:
4-175740842-AAAGGCATTTTT-A
gnomAD v4:
4-175740842-AAAGGCATTTTT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.175740849_175740859del , CM000666.2:g.175740849_175740859del | GRCh38 |
| NC_000004.11:g.176662000_176662010del , CM000666.1:g.176662000_176662010del | GRCh37 |
| NC_000004.10:g.176898994_176899004del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000393658.7:c.38-39086_38-39076del MANE Select | ENSP00000377268.2:n.38-39086_38-39076del | |
| ENST00000280187.11:c.38-39086_38-39076del | ENSP00000280187.7:n.38-39086_38-39076del | |
| ENST00000393658.6:c.38-39086_38-39076del | ENSP00000377268.2:n.38-39086_38-39076del | |
| ENST00000502754.5:c.-152-39086_-152-39076del | ENSP00000426821.1:n.-152-39086_-152-39076... | |
| ENST00000503397.5:c.14-39086_14-39076del | ENSP00000422959.1:n.14-39086_14-39076del | |
| ENST00000505304.1:c.17-39086_17-39076del | ENSP00000425463.1:n.17-39086_17-39076del | |
| ENST00000505375.5:c.-152-39086_-152-39076del | ENSP00000424125.1:n.-152-39086_-152-39076... | |
| ENST00000505561.5:c.-152-39086_-152-39076del | ENSP00000425409.1:n.-152-39086_-152-39076... | |
| ENST00000506894.5:c.5-39086_5-39076del | ENSP00000421578.1:n.5-39086_5-39076del | |
| ENST00000507520.5:c.-152-39086_-152-39076del | ENSP00000424075.1:n.-152-39086_-152-39076... | |
| ENST00000507540.1:c.-152-39086_-152-39076del | ENSP00000421407.1:n.-152-39086_-152-39076... | |
| ENST00000509865.5:c.-152-39086_-152-39076del | ENSP00000422712.1:n.-152-39086_-152-39076... | |
| ENST00000512509.5:c.-152-39086_-152-39076del | ENSP00000424443.1:n.-152-39086_-152-39076... | |
| ENST00000512610.5:c.-152-39086_-152-39076del | ENSP00000426984.1:n.-152-39086_-152-39076... | |
| ENST00000512897.5:c.-152-39086_-152-39076del | ENSP00000425925.1:n.-152-39086_-152-39076... | |
| ENST00000513365.1:c.38-39086_38-39076del | ENSP00000423122.1:n.38-39086_38-39076del | |
| ENST00000513667.5:c.-152-39086_-152-39076del | ENSP00000421373.1:n.-152-39086_-152-39076... | |
| ENST00000515090.5:c.17-39086_17-39076del | ENSP00000423984.1:n.17-39086_17-39076del | |
| NM_001261447.1:c.283-88866_283-88856del | NP_001248376.1:n.283-88866_283-88856del | |
| NM_001261448.1:c.17-39086_17-39076del | NP_001248377.1:n.17-39086_17-39076del | |
| NM_005277.4:c.38-39086_38-39076del | NP_005268.1:n.38-39086_38-39076del | |
| NM_201591.2:c.38-39086_38-39076del | NP_963885.1:n.38-39086_38-39076del | |
| NM_201592.2:c.5-39086_5-39076del | NP_963886.1:n.5-39086_5-39076del | |
| NR_048571.1:n.442+71338_442+71348del | ||
| XM_011531877.1:c.-152-39086_-152-39076del | XP_011530179.1:n.-152-39086_-152-39076del... | |
| NM_001388090.1:c.-152-39086_-152-39076del | NP_001375019.1:n.-152-39086_-152-39076del... | |
| NM_005277.5:c.38-39086_38-39076del | NP_005268.1:n.38-39086_38-39076del | |
| NM_201591.3:c.38-39086_38-39076del MANE Select | NP_963885.1:n.38-39086_38-39076del | |
| NM_201592.3:c.5-39086_5-39076del | NP_963886.1:n.5-39086_5-39076del |