Canonical Allele Identifier: CA2209082865

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948102G= , CM000678.2:g.13948102G=	GRCh38
NC_000016.9:g.14041959G= , CM000678.1:g.14041959G=	GRCh37
NC_000016.8:g.13949460G=	NCBI36
NG_011442.1:g.32946G= , LRG_463:g.32946G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2644G=	ENSP00000507912.1:p.Glu882=
ENST00000683962.1:c.*2200G=	ENSP00000506854.1:n.*2200G=
ENST00000311895.8:c.2506G= MANE Select	ENSP00000310520.7:p.Glu836=
ENST00000311895.7:c.2506G=	ENSP00000310520.7:p.Glu836=
ENST00000389138.7:n.1783G=
NM_005236.2:c.2506G= , LRG_463t1:c.2506G=	NP_005227.1:p.Glu836=
XM_011522424.1:c.2644G=	XP_011520726.1:p.Glu882=
XM_011522425.1:c.1963G=	XP_011520727.1:p.Glu655=
XM_011522426.1:c.1717G=	XP_011520728.1:p.Glu573=
XM_011522427.1:c.1156G=	XP_011520729.1:p.Glu386=
XR_932805.1:n.2665G=
XM_011522424.3:c.2644G=	XP_011520726.1:p.Glu882=
XM_017023043.2:c.1717G=	XP_016878532.1:p.Glu573=
NM_005236.3:c.2506G= MANE Select	NP_005227.1:p.Glu836=