Canonical Allele Identifier: CA376708831

Gene: ERCC6

Linked Data

• dbSNP Id: rs541909446
• gnomAD v3: 10-49461556-A-G
• gnomAD v4: 10-49461556-A-G
• MyVariant Identifiers: chr10:g.50669602A>G (hg19) ; chr10:g.49461556A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461556A>G , CM000672.2:g.49461556A>G	GRCh38
NC_000010.10:g.50669602A>G , CM000672.1:g.50669602A>G	GRCh37
NC_000010.9:g.50339608A>G	NCBI36
NG_009442.1:g.82546T>C , LRG_465:g.82546T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3779T>C MANE Select	ENSP00000348089.5:p.Val1260Ala
ENST00000679552.1:n.850T>C
ENST00000679871.1:n.925T>C
ENST00000679974.1:n.828T>C
ENST00000681632.1:n.5182T>C
ENST00000681659.1:c.3620T>C	ENSP00000505631.1:p.Val1207Ala
ENST00000355832.9:c.3779T>C	ENSP00000348089.5:p.Val1260Ala
ENST00000465653.1:n.101T>C
ENST00000623073.3:c.*2075T>C	ENSP00000485650.1:n.*2075T>C
ENST00000623115.3:c.1889T>C	ENSP00000485321.1:p.Val630Ala
ENST00000624341.3:c.1611T>C
NM_000124.3:c.3779T>C	NP_000115.1:p.Val1260Ala
XR_945953.1:n.243-10009A>G
NM_001346440.1:c.3779T>C	NP_001333369.1:p.Val1260Ala
NM_000124.4:c.3779T>C MANE Select	NP_000115.1:p.Val1260Ala
NM_001346440.2:c.3779T>C	NP_001333369.1:p.Val1260Ala