Canonical Allele Identifier: CA1908749400

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470416T= , CM000672.2:g.49470416T=	GRCh38
NC_000010.10:g.50678462T= , CM000672.1:g.50678462T=	GRCh37
NC_000010.9:g.50348468T=	NCBI36
NG_009442.1:g.73686A= , LRG_465:g.73686A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3544A= MANE Select	ENSP00000348089.5:p.Lys1182=
ENST00000679552.1:n.615A=
ENST00000679871.1:n.690A=
ENST00000679974.1:n.593A=
ENST00000681632.1:n.4947A=
ENST00000681659.1:c.3385A=	ENSP00000505631.1:p.Lys1129=
ENST00000355832.9:c.3544A=	ENSP00000348089.5:p.Lys1182=
ENST00000623073.3:c.*1840A=	ENSP00000485650.1:n.*1840A=
ENST00000623115.3:c.1654A=	ENSP00000485321.1:p.Lys552=
ENST00000624341.3:c.1376A=
NM_000124.3:c.3544A=	NP_000115.1:p.Lys1182=
XR_945953.1:n.243-1149T=
NM_001346440.1:c.3544A=	NP_001333369.1:p.Lys1182=
NM_000124.4:c.3544A= MANE Select	NP_000115.1:p.Lys1182=
NM_001346440.2:c.3544A=	NP_001333369.1:p.Lys1182=