Canonical Allele Identifier: CA2209082840

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948041G= , CM000678.2:g.13948041G=	GRCh38
NC_000016.9:g.14041898G= , CM000678.1:g.14041898G=	GRCh37
NC_000016.8:g.13949399G=	NCBI36
NG_011442.1:g.32885G= , LRG_463:g.32885G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2583G=	ENSP00000507912.1:p.Glu861=
ENST00000683962.1:c.*2139G=	ENSP00000506854.1:n.*2139G=
ENST00000311895.8:c.2445G= MANE Select	ENSP00000310520.7:p.Glu815=
ENST00000311895.7:c.2445G=	ENSP00000310520.7:p.Glu815=
ENST00000389138.7:n.1722G=
NM_005236.2:c.2445G= , LRG_463t1:c.2445G=	NP_005227.1:p.Glu815=
XM_011522424.1:c.2583G=	XP_011520726.1:p.Glu861=
XM_011522425.1:c.1902G=	XP_011520727.1:p.Glu634=
XM_011522426.1:c.1656G=	XP_011520728.1:p.Glu552=
XM_011522427.1:c.1095G=	XP_011520729.1:p.Glu365=
XR_932805.1:n.2604G=
XM_011522424.3:c.2583G=	XP_011520726.1:p.Glu861=
XM_017023043.2:c.1656G=	XP_016878532.1:p.Glu552=
NM_005236.3:c.2445G= MANE Select	NP_005227.1:p.Glu815=