Canonical Allele Identifier: CA376716897

Gene: ERCC6

Linked Data

• gnomAD v4: 10-49470832-G-C
• MyVariant Identifiers: chr10:g.50678878G>C (hg19) ; chr10:g.49470832G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470832G>C , CM000672.2:g.49470832G>C	GRCh38
NC_000010.10:g.50678878G>C , CM000672.1:g.50678878G>C	GRCh37
NC_000010.9:g.50348884G>C	NCBI36
NG_009442.1:g.73270C>G , LRG_465:g.73270C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3128C>G MANE Select	ENSP00000348089.5:p.Ala1043Gly
ENST00000679552.1:n.199C>G
ENST00000679871.1:n.274C>G
ENST00000679974.1:n.177C>G
ENST00000681632.1:n.4531C>G
ENST00000681659.1:c.2969C>G	ENSP00000505631.1:p.Ala990Gly
ENST00000355832.9:c.3128C>G	ENSP00000348089.5:p.Ala1043Gly
ENST00000623073.3:c.*1424C>G	ENSP00000485650.1:n.*1424C>G
ENST00000623115.3:c.1238C>G	ENSP00000485321.1:p.Ala413Gly
ENST00000624341.3:c.960C>G
NM_000124.3:c.3128C>G	NP_000115.1:p.Ala1043Gly
XR_945953.1:n.243-733G>C
NM_001346440.1:c.3128C>G	NP_001333369.1:p.Ala1043Gly
NM_000124.4:c.3128C>G MANE Select	NP_000115.1:p.Ala1043Gly
NM_001346440.2:c.3128C>G	NP_001333369.1:p.Ala1043Gly