Canonical Allele Identifier: CA1908772735

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493209C= , CM000672.2:g.49493209C=	GRCh38
NC_000010.10:g.50701255C= , CM000672.1:g.50701255C=	GRCh37
NC_000010.9:g.50371261C=	NCBI36
NG_009442.1:g.50893G= , LRG_465:g.50893G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.1729G= MANE Select	ENSP00000348089.5:p.Val577=
ENST00000681632.1:n.1807G=
ENST00000681659.1:c.1570G=	ENSP00000505631.1:p.Val524=
ENST00000355832.9:c.1729G=	ENSP00000348089.5:p.Val577=
ENST00000475116.1:n.275+7329G=
ENST00000623073.3:c.130G=	ENSP00000485650.1:p.Val44=
ENST00000623115.3:c.-70+7329G=	ENSP00000485321.1:n.-70+7329G=
ENST00000623318.1:c.130G=	ENSP00000485423.1:p.Val44=
NM_000124.3:c.1729G=	NP_000115.1:p.Val577=
NM_001346440.1:c.1729G=	NP_001333369.1:p.Val577=
NM_000124.4:c.1729G= MANE Select	NP_000115.1:p.Val577=
NM_001346440.2:c.1729G=	NP_001333369.1:p.Val577=