Canonical Allele Identifier: CA1908749597

Gene: ERCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49470854G= , CM000672.2:g.49470854G=	GRCh38
NC_000010.10:g.50678900G= , CM000672.1:g.50678900G=	GRCh37
NC_000010.9:g.50348906G=	NCBI36
NG_009442.1:g.73248C= , LRG_465:g.73248C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355832.10:c.3106C= MANE Select	ENSP00000348089.5:p.Leu1036=
ENST00000679552.1:n.177C=
ENST00000679871.1:n.252C=
ENST00000679974.1:n.155C=
ENST00000681632.1:n.4509C=
ENST00000681659.1:c.2947C=	ENSP00000505631.1:p.Leu983=
ENST00000355832.9:c.3106C=	ENSP00000348089.5:p.Leu1036=
ENST00000623073.3:c.*1402C=	ENSP00000485650.1:n.*1402C=
ENST00000623115.3:c.1216C=	ENSP00000485321.1:p.Leu406=
ENST00000624341.3:c.938C=
NM_000124.3:c.3106C=	NP_000115.1:p.Leu1036=
XR_945953.1:n.243-711G=
NM_001346440.1:c.3106C=	NP_001333369.1:p.Leu1036=
NM_000124.4:c.3106C= MANE Select	NP_000115.1:p.Leu1036=
NM_001346440.2:c.3106C=	NP_001333369.1:p.Leu1036=