Canonical Allele Identifier: CA469600373

Gene: ERCC6

Linked Data

• MyVariant Identifiers: chr10:g.50669541T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49461495T>A , CM000672.2:g.49461495T>A	GRCh38
NC_000010.10:g.50669541T>A , CM000672.1:g.50669541T>A	GRCh37
NC_000010.9:g.50339547T>A	NCBI36
NG_009442.1:g.82607A>T , LRG_465:g.82607A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3840A>T MANE Select	ENSP00000348089.5:p.Val1280=
ENST00000679552.1:n.911A>T
ENST00000679871.1:n.986A>T
ENST00000679974.1:n.889A>T
ENST00000681632.1:n.5243A>T
ENST00000681659.1:c.3681A>T	ENSP00000505631.1:p.Val1227=
ENST00000355832.9:c.3840A>T	ENSP00000348089.5:p.Val1280=
ENST00000465653.1:n.162A>T
ENST00000623073.3:c.*2136A>T	ENSP00000485650.1:n.*2136A>T
ENST00000623115.3:c.1950A>T	ENSP00000485321.1:p.Val650=
ENST00000624341.3:c.1672A>T
NM_000124.3:c.3840A>T	NP_000115.1:p.Val1280=
XR_945953.1:n.243-10070T>A
NM_001346440.1:c.3840A>T	NP_001333369.1:p.Val1280=
NM_000124.4:c.3840A>T MANE Select	NP_000115.1:p.Val1280=
NM_001346440.2:c.3840A>T	NP_001333369.1:p.Val1280=