Canonical Allele Identifier: CA1908760328

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49482771T= , CM000672.2:g.49482771T=	GRCh38
NC_000010.10:g.50690817T= , CM000672.1:g.50690817T=	GRCh37
NC_000010.9:g.50360823T=	NCBI36
NG_009442.1:g.61331A= , LRG_465:g.61331A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.2085A= MANE Select	ENSP00000348089.5:p.Gly695=
ENST00000681632.1:n.2163A=
ENST00000681659.1:c.1926A=	ENSP00000505631.1:p.Gly642=
ENST00000355832.9:c.2085A=	ENSP00000348089.5:p.Gly695=
ENST00000623073.3:c.*477A=	ENSP00000485650.1:n.*477A=
ENST00000623115.3:c.195A=	ENSP00000485321.1:p.Gly65=
NM_000124.3:c.2085A=	NP_000115.1:p.Gly695=
NM_001346440.1:c.2085A=	NP_001333369.1:p.Gly695=
NM_000124.4:c.2085A= MANE Select	NP_000115.1:p.Gly695=
NM_001346440.2:c.2085A=	NP_001333369.1:p.Gly695=