Canonical Allele Identifier: CA2209082700

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947771G= , CM000678.2:g.13947771G=	GRCh38
NC_000016.9:g.14041628G= , CM000678.1:g.14041628G=	GRCh37
NC_000016.8:g.13949129G=	NCBI36
NG_011442.1:g.32615G= , LRG_463:g.32615G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2313G=	ENSP00000507912.1:p.Glu771=
ENST00000683962.1:c.*1869G=	ENSP00000506854.1:n.*1869G=
ENST00000311895.8:c.2175G= MANE Select	ENSP00000310520.7:p.Glu725=
ENST00000311895.7:c.2175G=	ENSP00000310520.7:p.Glu725=
ENST00000389138.7:n.1452G=
ENST00000462862.1:c.488G=	ENSP00000461322.1:n.488G=
NM_005236.2:c.2175G= , LRG_463t1:c.2175G=	NP_005227.1:p.Glu725=
XM_011522424.1:c.2313G=	XP_011520726.1:p.Glu771=
XM_011522425.1:c.1632G=	XP_011520727.1:p.Glu544=
XM_011522426.1:c.1386G=	XP_011520728.1:p.Glu462=
XM_011522427.1:c.825G=	XP_011520729.1:p.Glu275=
XR_932805.1:n.2334G=
XM_011522424.3:c.2313G=	XP_011520726.1:p.Glu771=
XM_017023043.2:c.1386G=	XP_016878532.1:p.Glu462=
NM_005236.3:c.2175G= MANE Select	NP_005227.1:p.Glu725=