Canonical Allele Identifier: CA1908778514

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49500592G= , CM000672.2:g.49500592G=	GRCh38
NC_000010.10:g.50708638G= , CM000672.1:g.50708638G=	GRCh37
NC_000010.9:g.50378644G=	NCBI36
NG_009442.1:g.43510C= , LRG_465:g.43510C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1631C= MANE Select	ENSP00000348089.5:p.Ala544=
ENST00000681632.1:n.1709C=
ENST00000681659.1:c.1526+5292C=	ENSP00000505631.1:n.1526+5292C=
ENST00000355832.9:c.1631C=	ENSP00000348089.5:p.Ala544=
ENST00000475116.1:n.221C=
ENST00000623073.3:c.32C=	ENSP00000485650.1:p.Ala11=
ENST00000623115.3:c.-124C=	ENSP00000485321.1:n.-124C=
ENST00000623318.1:c.32C=	ENSP00000485423.1:p.Ala11=
NM_000124.3:c.1631C=	NP_000115.1:p.Ala544=
NM_001346440.1:c.1631C=	NP_001333369.1:p.Ala544=
NM_000124.4:c.1631C= MANE Select	NP_000115.1:p.Ala544=
NM_001346440.2:c.1631C=	NP_001333369.1:p.Ala544=