Canonical Allele Identifier: CA1908760080

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49482689G= , CM000672.2:g.49482689G=	GRCh38
NC_000010.10:g.50690735G= , CM000672.1:g.50690735G=	GRCh37
NC_000010.9:g.50360741G=	NCBI36
NG_009442.1:g.61413C= , LRG_465:g.61413C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.2167C= MANE Select	ENSP00000348089.5:p.Gln723=
ENST00000681632.1:n.2245C=
ENST00000681659.1:c.2008C=	ENSP00000505631.1:p.Gln670=
ENST00000355832.9:c.2167C=	ENSP00000348089.5:p.Gln723=
ENST00000623073.3:c.*559C=	ENSP00000485650.1:n.*559C=
ENST00000623115.3:c.277C=	ENSP00000485321.1:p.Gln93=
NM_000124.3:c.2167C=	NP_000115.1:p.Gln723=
NM_001346440.1:c.2167C=	NP_001333369.1:p.Gln723=
NM_000124.4:c.2167C= MANE Select	NP_000115.1:p.Gln723=
NM_001346440.2:c.2167C=	NP_001333369.1:p.Gln723=