Canonical Allele Identifier: CA1908749382

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470390C= , CM000672.2:g.49470390C=	GRCh38
NC_000010.10:g.50678436C= , CM000672.1:g.50678436C=	GRCh37
NC_000010.9:g.50348442C=	NCBI36
NG_009442.1:g.73712G= , LRG_465:g.73712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3570G= MANE Select	ENSP00000348089.5:p.Val1190=
ENST00000679552.1:n.641G=
ENST00000679871.1:n.716G=
ENST00000679974.1:n.619G=
ENST00000681632.1:n.4973G=
ENST00000681659.1:c.3411G=	ENSP00000505631.1:p.Val1137=
ENST00000355832.9:c.3570G=	ENSP00000348089.5:p.Val1190=
ENST00000623073.3:c.*1866G=	ENSP00000485650.1:n.*1866G=
ENST00000623115.3:c.1680G=	ENSP00000485321.1:p.Val560=
ENST00000624341.3:c.1402G=
NM_000124.3:c.3570G=	NP_000115.1:p.Val1190=
XR_945953.1:n.243-1175C=
NM_001346440.1:c.3570G=	NP_001333369.1:p.Val1190=
NM_000124.4:c.3570G= MANE Select	NP_000115.1:p.Val1190=
NM_001346440.2:c.3570G=	NP_001333369.1:p.Val1190=