Linked Data
dbSNP Id:
rs1160663201
gnomAD v2:
13-103527964-C-T
gnomAD v3:
13-102875614-C-T
gnomAD v4:
13-102875614-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.102875614C>T , CM000675.2:g.102875614C>T | GRCh38 |
| NC_000013.10:g.103527964C>T , CM000675.1:g.103527964C>T | GRCh37 |
| NC_000013.9:g.102325965C>T | NCBI36 |
| NG_007146.1:g.34791C>T , LRG_464:g.34791C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682632.1:n.4373C>T (ERCC5) | ||
| ENST00000682869.1:n.3921C>T (ERCC5) | ||
| ENST00000683246.1:n.4909C>T (ERCC5) | ||
| ENST00000683642.1:n.3502C>T (ERCC5) | ||
| ENST00000639132.1:c.3947C>T (BIVM-ERCC5) | ENSP00000492684.1:p.Thr1316Ile | |
| ENST00000639435.1:c.4634C>T (BIVM-ERCC5) | ENSP00000491742.1:p.Thr1545Ile | |
| ENST00000651002.1:c.*3033C>T (ERCC5) | ENSP00000498809.1:n.*3033C>T | |
| ENST00000651055.1:n.3399C>T (ERCC5) | ||
| ENST00000651281.1:n.3640C>T (ERCC5) | ||
| ENST00000651387.1:n.2756C>T (ERCC5) | ||
| ENST00000651470.1:c.*444C>T (ERCC5) | ENSP00000498701.1:n.*444C>T | |
| ENST00000652225.2:c.3272C>T (ERCC5) MANE Select | ENSP00000498881.2:p.Thr1091Ile | |
| ENST00000652613.1:c.2768C>T (ERCC5) | ENSP00000498357.1:p.Thr923Ile | |
| ENST00000355739.8:c.3272C>T (ERCC5) | ENSP00000347978.4:p.Thr1091Ile | |
| ENST00000375954.1:c.971C>T (ERCC5) | ENSP00000365121.1:p.Thr324Ile | |
| ENST00000472247.1:n.432C>T (ERCC5) | ||
| ENST00000610537.4:c.3269C>T (ERCC5) | ENSP00000478667.1:p.Thr1090Ile | |
| NM_000123.3:c.3272C>T , LRG_464t1:c.3272C>T (ERCC5) | NP_000114.2:p.Thr1091Ile | |
| NM_001204425.1:c.4634C>T (BIVM-ERCC5) | NP_001191354.1:p.Thr1545Ile | |
| NM_000123.4:c.3272C>T (ERCC5) MANE Select | NP_000114.3:p.Thr1091Ile | |
| NM_001204425.2:c.4634C>T (BIVM-ERCC5) | NP_001191354.2:p.Thr1545Ile |