Canonical Allele Identifier: CA1908749677

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49471010G= , CM000672.2:g.49471010G=	GRCh38
NC_000010.10:g.50679056G= , CM000672.1:g.50679056G=	GRCh37
NC_000010.9:g.50349062G=	NCBI36
NG_009442.1:g.73092C= , LRG_465:g.73092C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3035C= MANE Select	ENSP00000348089.5:p.Ala1012=
ENST00000679552.1:n.142-121C=
ENST00000679871.1:n.181C=
ENST00000679974.1:n.120-121C=
ENST00000681632.1:n.4438C=
ENST00000681659.1:c.2876C=	ENSP00000505631.1:p.Ala959=
ENST00000355832.9:c.3035C=	ENSP00000348089.5:p.Ala1012=
ENST00000623073.3:c.*1331C=	ENSP00000485650.1:n.*1331C=
ENST00000623115.3:c.1145C=	ENSP00000485321.1:p.Ala382=
ENST00000624341.3:c.867C=
NM_000124.3:c.3035C=	NP_000115.1:p.Ala1012=
XR_945953.1:n.243-555G=
NM_001346440.1:c.3035C=	NP_001333369.1:p.Ala1012=
NM_000124.4:c.3035C= MANE Select	NP_000115.1:p.Ala1012=
NM_001346440.2:c.3035C=	NP_001333369.1:p.Ala1012=