Canonical Allele Identifier: CA2209082750

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947878T= , CM000678.2:g.13947878T=	GRCh38
NC_000016.9:g.14041735T= , CM000678.1:g.14041735T=	GRCh37
NC_000016.8:g.13949236T=	NCBI36
NG_011442.1:g.32722T= , LRG_463:g.32722T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2420T=	ENSP00000507912.1:p.Phe807=
ENST00000683962.1:c.*1976T=	ENSP00000506854.1:n.*1976T=
ENST00000311895.8:c.2282T= MANE Select	ENSP00000310520.7:p.Phe761=
ENST00000311895.7:c.2282T=	ENSP00000310520.7:p.Phe761=
ENST00000389138.7:n.1559T=
ENST00000462862.1:c.595T=	ENSP00000461322.1:n.595T=
NM_005236.2:c.2282T= , LRG_463t1:c.2282T=	NP_005227.1:p.Phe761=
XM_011522424.1:c.2420T=	XP_011520726.1:p.Phe807=
XM_011522425.1:c.1739T=	XP_011520727.1:p.Phe580=
XM_011522426.1:c.1493T=	XP_011520728.1:p.Phe498=
XM_011522427.1:c.932T=	XP_011520729.1:p.Phe311=
XR_932805.1:n.2441T=
XM_011522424.3:c.2420T=	XP_011520726.1:p.Phe807=
XM_017023043.2:c.1493T=	XP_016878532.1:p.Phe498=
NM_005236.3:c.2282T= MANE Select	NP_005227.1:p.Phe761=