Linked Data
dbSNP Id:
rs775348948
ExAC:
13:103525614 G / A
gnomAD v2:
13-103525614-G-A
gnomAD v3:
13-102873264-G-A
gnomAD v4:
13-102873264-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.102873264G>A , CM000675.2:g.102873264G>A | GRCh38 |
| NC_000013.10:g.103525614G>A , CM000675.1:g.103525614G>A | GRCh37 |
| NC_000013.9:g.102323615G>A | NCBI36 |
| NG_007146.1:g.32441G>A , LRG_464:g.32441G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682632.1:n.3986G>A (ERCC5) | ||
| ENST00000682869.1:n.3534G>A (ERCC5) | ||
| ENST00000683246.1:n.4522G>A (ERCC5) | ||
| ENST00000683642.1:n.3115G>A (ERCC5) | ||
| ENST00000639132.1:c.3560G>A (BIVM-ERCC5) | ENSP00000492684.1:p.Cys1187Tyr | |
| ENST00000639435.1:c.4247G>A (BIVM-ERCC5) | ENSP00000491742.1:p.Cys1416Tyr | |
| ENST00000651002.1:c.*2646G>A (ERCC5) | ENSP00000498809.1:n.*2646G>A | |
| ENST00000651055.1:n.3012G>A (ERCC5) | ||
| ENST00000651281.1:n.3253G>A (ERCC5) | ||
| ENST00000651387.1:n.2369G>A (ERCC5) | ||
| ENST00000651470.1:c.*57G>A (ERCC5) | ENSP00000498701.1:n.*57G>A | |
| ENST00000652225.2:c.2885G>A (ERCC5) MANE Select | ENSP00000498881.2:p.Cys962Tyr | |
| ENST00000652613.1:c.2381G>A (ERCC5) | ENSP00000498357.1:p.Cys794Tyr | |
| ENST00000355739.8:c.2885G>A (ERCC5) | ENSP00000347978.4:p.Cys962Tyr | |
| ENST00000375954.1:c.584G>A (ERCC5) | ENSP00000365121.1:p.Cys195Tyr | |
| ENST00000610537.4:c.2882G>A (ERCC5) | ENSP00000478667.1:p.Cys961Tyr | |
| NM_000123.3:c.2885G>A , LRG_464t1:c.2885G>A (ERCC5) | NP_000114.2:p.Cys962Tyr | |
| NM_001204425.1:c.4247G>A (BIVM-ERCC5) | NP_001191354.1:p.Cys1416Tyr | |
| NM_000123.4:c.2885G>A (ERCC5) MANE Select | NP_000114.3:p.Cys962Tyr | |
| NM_001204425.2:c.4247G>A (BIVM-ERCC5) | NP_001191354.2:p.Cys1416Tyr |