Canonical Allele Identifier: CA2209082773

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947905C= , CM000678.2:g.13947905C=	GRCh38
NC_000016.9:g.14041762C= , CM000678.1:g.14041762C=	GRCh37
NC_000016.8:g.13949263C=	NCBI36
NG_011442.1:g.32749C= , LRG_463:g.32749C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2447C=	ENSP00000507912.1:p.Thr816=
ENST00000683962.1:c.*2003C=	ENSP00000506854.1:n.*2003C=
ENST00000311895.8:c.2309C= MANE Select	ENSP00000310520.7:p.Thr770=
ENST00000311895.7:c.2309C=	ENSP00000310520.7:p.Thr770=
ENST00000389138.7:n.1586C=
ENST00000462862.1:c.622C=	ENSP00000461322.1:n.622C=
NM_005236.2:c.2309C= , LRG_463t1:c.2309C=	NP_005227.1:p.Thr770=
XM_011522424.1:c.2447C=	XP_011520726.1:p.Thr816=
XM_011522425.1:c.1766C=	XP_011520727.1:p.Thr589=
XM_011522426.1:c.1520C=	XP_011520728.1:p.Thr507=
XM_011522427.1:c.959C=	XP_011520729.1:p.Thr320=
XR_932805.1:n.2468C=
XM_011522424.3:c.2447C=	XP_011520726.1:p.Thr816=
XM_017023043.2:c.1520C=	XP_016878532.1:p.Thr507=
NM_005236.3:c.2309C= MANE Select	NP_005227.1:p.Thr770=