Canonical Allele Identifier: CA1908749558

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470773C= , CM000672.2:g.49470773C=	GRCh38
NC_000010.10:g.50678819C= , CM000672.1:g.50678819C=	GRCh37
NC_000010.9:g.50348825C=	NCBI36
NG_009442.1:g.73329G= , LRG_465:g.73329G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3187G= MANE Select	ENSP00000348089.5:p.Val1063=
ENST00000679552.1:n.258G=
ENST00000679871.1:n.333G=
ENST00000679974.1:n.236G=
ENST00000681632.1:n.4590G=
ENST00000681659.1:c.3028G=	ENSP00000505631.1:p.Val1010=
ENST00000355832.9:c.3187G=	ENSP00000348089.5:p.Val1063=
ENST00000623073.3:c.*1483G=	ENSP00000485650.1:n.*1483G=
ENST00000623115.3:c.1297G=	ENSP00000485321.1:p.Val433=
ENST00000624341.3:c.1019G=
NM_000124.3:c.3187G=	NP_000115.1:p.Val1063=
XR_945953.1:n.243-792C=
NM_001346440.1:c.3187G=	NP_001333369.1:p.Val1063=
NM_000124.4:c.3187G= MANE Select	NP_000115.1:p.Val1063=
NM_001346440.2:c.3187G=	NP_001333369.1:p.Val1063=