Canonical Allele Identifier: CA2209082745

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947857G= , CM000678.2:g.13947857G=	GRCh38
NC_000016.9:g.14041714G= , CM000678.1:g.14041714G=	GRCh37
NC_000016.8:g.13949215G=	NCBI36
NG_011442.1:g.32701G= , LRG_463:g.32701G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2399G=	ENSP00000507912.1:p.Arg800=
ENST00000683962.1:c.*1955G=	ENSP00000506854.1:n.*1955G=
ENST00000311895.8:c.2261G= MANE Select	ENSP00000310520.7:p.Arg754=
ENST00000311895.7:c.2261G=	ENSP00000310520.7:p.Arg754=
ENST00000389138.7:n.1538G=
ENST00000462862.1:c.574G=	ENSP00000461322.1:n.574G=
NM_005236.2:c.2261G= , LRG_463t1:c.2261G=	NP_005227.1:p.Arg754=
XM_011522424.1:c.2399G=	XP_011520726.1:p.Arg800=
XM_011522425.1:c.1718G=	XP_011520727.1:p.Arg573=
XM_011522426.1:c.1472G=	XP_011520728.1:p.Arg491=
XM_011522427.1:c.911G=	XP_011520729.1:p.Arg304=
XR_932805.1:n.2420G=
XM_011522424.3:c.2399G=	XP_011520726.1:p.Arg800=
XM_017023043.2:c.1472G=	XP_016878532.1:p.Arg491=
NM_005236.3:c.2261G= MANE Select	NP_005227.1:p.Arg754=