Canonical Allele Identifier: CA2209082849

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948062G= , CM000678.2:g.13948062G=	GRCh38
NC_000016.9:g.14041919G= , CM000678.1:g.14041919G=	GRCh37
NC_000016.8:g.13949420G=	NCBI36
NG_011442.1:g.32906G= , LRG_463:g.32906G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2604G=	ENSP00000507912.1:p.Gln868=
ENST00000683962.1:c.*2160G=	ENSP00000506854.1:n.*2160G=
ENST00000311895.8:c.2466G= MANE Select	ENSP00000310520.7:p.Gln822=
ENST00000311895.7:c.2466G=	ENSP00000310520.7:p.Gln822=
ENST00000389138.7:n.1743G=
NM_005236.2:c.2466G= , LRG_463t1:c.2466G=	NP_005227.1:p.Gln822=
XM_011522424.1:c.2604G=	XP_011520726.1:p.Gln868=
XM_011522425.1:c.1923G=	XP_011520727.1:p.Gln641=
XM_011522426.1:c.1677G=	XP_011520728.1:p.Gln559=
XM_011522427.1:c.1116G=	XP_011520729.1:p.Gln372=
XR_932805.1:n.2625G=
XM_011522424.3:c.2604G=	XP_011520726.1:p.Gln868=
XM_017023043.2:c.1677G=	XP_016878532.1:p.Gln559=
NM_005236.3:c.2466G= MANE Select	NP_005227.1:p.Gln822=