Canonical Allele Identifier: CA2209081418

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944765A= , CM000678.2:g.13944765A=	GRCh38
NC_000016.9:g.14038622A= , CM000678.1:g.14038622A=	GRCh37
NC_000016.8:g.13946123A=	NCBI36
NG_011442.1:g.29609A= , LRG_463:g.29609A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2085A=	ENSP00000507912.1:p.Arg695=
ENST00000683962.1:c.*1641A=	ENSP00000506854.1:n.*1641A=
ENST00000311895.8:c.1947A= MANE Select	ENSP00000310520.7:p.Arg649=
ENST00000311895.7:c.1947A=	ENSP00000310520.7:p.Arg649=
ENST00000389138.7:n.1224A=
ENST00000462862.1:c.260A=	ENSP00000461322.1:n.260A=
NM_005236.2:c.1947A= , LRG_463t1:c.1947A=	NP_005227.1:p.Arg649=
XM_011522424.1:c.2085A=	XP_011520726.1:p.Arg695=
XM_011522425.1:c.1404A=	XP_011520727.1:p.Arg468=
XM_011522426.1:c.1158A=	XP_011520728.1:p.Arg386=
XM_011522427.1:c.597A=	XP_011520729.1:p.Arg199=
XR_932805.1:n.2106A=
XM_011522424.3:c.2085A=	XP_011520726.1:p.Arg695=
XM_017023043.2:c.1158A=	XP_016878532.1:p.Arg386=
NM_005236.3:c.1947A= MANE Select	NP_005227.1:p.Arg649=