Canonical Allele Identifier: CA2209073547

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935731G= , CM000678.2:g.13935731G=	GRCh38
NC_000016.9:g.14029588G= , CM000678.1:g.14029588G=	GRCh37
NC_000016.8:g.13937089G=	NCBI36
NG_011442.1:g.20575G= , LRG_463:g.20575G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1877G=
ENST00000682617.1:c.1937G=	ENSP00000507912.1:p.Gly646=
ENST00000682826.1:c.*1113G=	ENSP00000507274.1:n.*1113G=
ENST00000682909.1:n.3839G=
ENST00000683277.1:n.3444G=
ENST00000683407.1:n.1807G=
ENST00000683962.1:c.*1493G=	ENSP00000506854.1:n.*1493G=
ENST00000311895.8:c.1799G= MANE Select	ENSP00000310520.7:p.Gly600=
ENST00000311895.7:c.1799G=	ENSP00000310520.7:p.Gly600=
ENST00000389138.7:n.1076G=
NM_005236.2:c.1799G= , LRG_463t1:c.1799G=	NP_005227.1:p.Gly600=
XM_011522424.1:c.1937G=	XP_011520726.1:p.Gly646=
XM_011522425.1:c.1256G=	XP_011520727.1:p.Gly419=
XM_011522426.1:c.1010G=	XP_011520728.1:p.Gly337=
XM_011522427.1:c.449G=	XP_011520729.1:p.Gly150=
XR_932805.1:n.1958G=
XM_011522424.3:c.1937G=	XP_011520726.1:p.Gly646=
XM_017023043.2:c.1010G=	XP_016878532.1:p.Gly337=
NM_005236.3:c.1799G= MANE Select	NP_005227.1:p.Gly600=