Canonical Allele Identifier: CA2209081411

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944748G= , CM000678.2:g.13944748G=	GRCh38
NC_000016.9:g.14038605G= , CM000678.1:g.14038605G=	GRCh37
NC_000016.8:g.13946106G=	NCBI36
NG_011442.1:g.29592G= , LRG_463:g.29592G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2068G=	ENSP00000507912.1:p.Glu690=
ENST00000683962.1:c.*1624G=	ENSP00000506854.1:n.*1624G=
ENST00000311895.8:c.1930G= MANE Select	ENSP00000310520.7:p.Glu644=
ENST00000311895.7:c.1930G=	ENSP00000310520.7:p.Glu644=
ENST00000389138.7:n.1207G=
ENST00000462862.1:c.243G=	ENSP00000461322.1:n.243G=
NM_005236.2:c.1930G= , LRG_463t1:c.1930G=	NP_005227.1:p.Glu644=
XM_011522424.1:c.2068G=	XP_011520726.1:p.Glu690=
XM_011522425.1:c.1387G=	XP_011520727.1:p.Glu463=
XM_011522426.1:c.1141G=	XP_011520728.1:p.Glu381=
XM_011522427.1:c.580G=	XP_011520729.1:p.Glu194=
XR_932805.1:n.2089G=
XM_011522424.3:c.2068G=	XP_011520726.1:p.Glu690=
XM_017023043.2:c.1141G=	XP_016878532.1:p.Glu381=
NM_005236.3:c.1930G= MANE Select	NP_005227.1:p.Glu644=