Canonical Allele Identifier: CA2209082935

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948242C= , CM000678.2:g.13948242C=	GRCh38
NC_000016.9:g.14042099C= , CM000678.1:g.14042099C=	GRCh37
NC_000016.8:g.13949600C=	NCBI36
NG_011442.1:g.33086C= , LRG_463:g.33086C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2784C=	ENSP00000507912.1:p.Asp928=
ENST00000683962.1:c.*2340C=	ENSP00000506854.1:n.*2340C=
ENST00000311895.8:c.2646C= MANE Select	ENSP00000310520.7:p.Asp882=
ENST00000311895.7:c.2646C=	ENSP00000310520.7:p.Asp882=
ENST00000389138.7:n.1923C=
NM_005236.2:c.2646C= , LRG_463t1:c.2646C=	NP_005227.1:p.Asp882=
XM_011522424.1:c.2784C=	XP_011520726.1:p.Asp928=
XM_011522425.1:c.2103C=	XP_011520727.1:p.Asp701=
XM_011522426.1:c.1857C=	XP_011520728.1:p.Asp619=
XM_011522427.1:c.1296C=	XP_011520729.1:p.Asp432=
XR_932805.1:n.2805C=
XM_011522424.3:c.2784C=	XP_011520726.1:p.Asp928=
XM_017023043.2:c.1857C=	XP_016878532.1:p.Asp619=
NM_005236.3:c.2646C= MANE Select	NP_005227.1:p.Asp882=