Canonical Allele Identifier: CA2209073515

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935698G= , CM000678.2:g.13935698G=	GRCh38
NC_000016.9:g.14029555G= , CM000678.1:g.14029555G=	GRCh37
NC_000016.8:g.13937056G=	NCBI36
NG_011442.1:g.20542G= , LRG_463:g.20542G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1844G=
ENST00000682617.1:c.1904G=	ENSP00000507912.1:p.Arg635=
ENST00000682826.1:c.*1080G=	ENSP00000507274.1:n.*1080G=
ENST00000682909.1:n.3806G=
ENST00000683277.1:n.3411G=
ENST00000683407.1:n.1774G=
ENST00000683962.1:c.*1460G=	ENSP00000506854.1:n.*1460G=
ENST00000311895.8:c.1766G= MANE Select	ENSP00000310520.7:p.Arg589=
ENST00000311895.7:c.1766G=	ENSP00000310520.7:p.Arg589=
ENST00000389138.7:n.1043G=
NM_005236.2:c.1766G= , LRG_463t1:c.1766G=	NP_005227.1:p.Arg589=
XM_011522424.1:c.1904G=	XP_011520726.1:p.Arg635=
XM_011522425.1:c.1223G=	XP_011520727.1:p.Arg408=
XM_011522426.1:c.977G=	XP_011520728.1:p.Arg326=
XM_011522427.1:c.416G=	XP_011520729.1:p.Arg139=
XR_932805.1:n.1925G=
XM_011522424.3:c.1904G=	XP_011520726.1:p.Arg635=
XM_017023043.2:c.977G=	XP_016878532.1:p.Arg326=
NM_005236.3:c.1766G= MANE Select	NP_005227.1:p.Arg589=