Canonical Allele Identifier: CA2209073490

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935690C= , CM000678.2:g.13935690C=	GRCh38
NC_000016.9:g.14029547C= , CM000678.1:g.14029547C=	GRCh37
NC_000016.8:g.13937048C=	NCBI36
NG_011442.1:g.20534C= , LRG_463:g.20534C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1836C=
ENST00000682617.1:c.1896C=	ENSP00000507912.1:p.Thr632=
ENST00000682826.1:c.*1072C=	ENSP00000507274.1:n.*1072C=
ENST00000682909.1:n.3798C=
ENST00000683277.1:n.3403C=
ENST00000683407.1:n.1766C=
ENST00000683962.1:c.*1452C=	ENSP00000506854.1:n.*1452C=
ENST00000311895.8:c.1758C= MANE Select	ENSP00000310520.7:p.Thr586=
ENST00000311895.7:c.1758C=	ENSP00000310520.7:p.Thr586=
ENST00000389138.7:n.1035C=
NM_005236.2:c.1758C= , LRG_463t1:c.1758C=	NP_005227.1:p.Thr586=
XM_011522424.1:c.1896C=	XP_011520726.1:p.Thr632=
XM_011522425.1:c.1215C=	XP_011520727.1:p.Thr405=
XM_011522426.1:c.969C=	XP_011520728.1:p.Thr323=
XM_011522427.1:c.408C=	XP_011520729.1:p.Thr136=
XR_932805.1:n.1917C=
XM_011522424.3:c.1896C=	XP_011520726.1:p.Thr632=
XM_017023043.2:c.969C=	XP_016878532.1:p.Thr323=
NM_005236.3:c.1758C= MANE Select	NP_005227.1:p.Thr586=