Canonical Allele Identifier: CA376714920

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50678578C>A (hg19) ; chr10:g.49470532C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470532C>A , CM000672.2:g.49470532C>A	GRCh38
NC_000010.10:g.50678578C>A , CM000672.1:g.50678578C>A	GRCh37
NC_000010.9:g.50348584C>A	NCBI36
NG_009442.1:g.73570G>T , LRG_465:g.73570G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3428G>T MANE Select	ENSP00000348089.5:p.Gly1143Val
ENST00000679552.1:n.499G>T
ENST00000679871.1:n.574G>T
ENST00000679974.1:n.477G>T
ENST00000681632.1:n.4831G>T
ENST00000681659.1:c.3269G>T	ENSP00000505631.1:p.Gly1090Val
ENST00000355832.9:c.3428G>T	ENSP00000348089.5:p.Gly1143Val
ENST00000623073.3:c.*1724G>T	ENSP00000485650.1:n.*1724G>T
ENST00000623115.3:c.1538G>T	ENSP00000485321.1:p.Gly513Val
ENST00000624341.3:c.1260G>T
NM_000124.3:c.3428G>T	NP_000115.1:p.Gly1143Val
XR_945953.1:n.243-1033C>A
NM_001346440.1:c.3428G>T	NP_001333369.1:p.Gly1143Val
NM_000124.4:c.3428G>T MANE Select	NP_000115.1:p.Gly1143Val
NM_001346440.2:c.3428G>T	NP_001333369.1:p.Gly1143Val