Canonical Allele Identifier: CA3218600727

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947887G= , CM000678.2:g.13947887G=	GRCh38
NC_000016.9:g.14041744G= , CM000678.1:g.14041744G=	GRCh37
NC_000016.8:g.13949245G=	NCBI36
NG_011442.1:g.32731G= , LRG_463:g.32731G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2291G= MANE Select	NP_005227.1:p.Ser764=
ENST00000311895.8:c.2291G= MANE Select	ENSP00000310520.7:p.Ser764=
NM_005236.2:c.2291G= , LRG_463t1:c.2291G=	NP_005227.1:p.Ser764=
ENST00000311895.7:c.2291G=	ENSP00000310520.7:p.Ser764=
ENST00000389138.7:n.1568G=
ENST00000462862.1:c.604G=	ENSP00000461322.1:n.604G=
ENST00000682617.1:c.2429G=	ENSP00000507912.1:p.Ser810=
ENST00000683962.1:c.*1985G=	ENSP00000506854.1:n.*1985G=
XM_011522424.1:c.2429G=	XP_011520726.1:p.Ser810=
XM_011522424.3:c.2429G=	XP_011520726.1:p.Ser810=
XM_011522425.1:c.1748G=	XP_011520727.1:p.Ser583=
XM_011522426.1:c.1502G=	XP_011520728.1:p.Ser501=
XM_011522427.1:c.941G=	XP_011520729.1:p.Ser314=
XM_017023043.2:c.1502G=	XP_016878532.1:p.Ser501=
XR_932805.1:n.2450G=