Canonical Allele Identifier: CA1908749425

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470471A= , CM000672.2:g.49470471A=	GRCh38
NC_000010.10:g.50678517A= , CM000672.1:g.50678517A=	GRCh37
NC_000010.9:g.50348523A=	NCBI36
NG_009442.1:g.73631T= , LRG_465:g.73631T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3489T= MANE Select	ENSP00000348089.5:p.Ala1163=
ENST00000679552.1:n.560T=
ENST00000679871.1:n.635T=
ENST00000679974.1:n.538T=
ENST00000681632.1:n.4892T=
ENST00000681659.1:c.3330T=	ENSP00000505631.1:p.Ala1110=
ENST00000355832.9:c.3489T=	ENSP00000348089.5:p.Ala1163=
ENST00000623073.3:c.*1785T=	ENSP00000485650.1:n.*1785T=
ENST00000623115.3:c.1599T=	ENSP00000485321.1:p.Ala533=
ENST00000624341.3:c.1321T=
NM_000124.3:c.3489T=	NP_000115.1:p.Ala1163=
XR_945953.1:n.243-1094A=
NM_001346440.1:c.3489T=	NP_001333369.1:p.Ala1163=
NM_000124.4:c.3489T= MANE Select	NP_000115.1:p.Ala1163=
NM_001346440.2:c.3489T=	NP_001333369.1:p.Ala1163=