Canonical Allele Identifier: CA2209082767

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947897C= , CM000678.2:g.13947897C=	GRCh38
NC_000016.9:g.14041754C= , CM000678.1:g.14041754C=	GRCh37
NC_000016.8:g.13949255C=	NCBI36
NG_011442.1:g.32741C= , LRG_463:g.32741C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2439C=	ENSP00000507912.1:p.Phe813=
ENST00000683962.1:c.*1995C=	ENSP00000506854.1:n.*1995C=
ENST00000311895.8:c.2301C= MANE Select	ENSP00000310520.7:p.Phe767=
ENST00000311895.7:c.2301C=	ENSP00000310520.7:p.Phe767=
ENST00000389138.7:n.1578C=
ENST00000462862.1:c.614C=	ENSP00000461322.1:n.614C=
NM_005236.2:c.2301C= , LRG_463t1:c.2301C=	NP_005227.1:p.Phe767=
XM_011522424.1:c.2439C=	XP_011520726.1:p.Phe813=
XM_011522425.1:c.1758C=	XP_011520727.1:p.Phe586=
XM_011522426.1:c.1512C=	XP_011520728.1:p.Phe504=
XM_011522427.1:c.951C=	XP_011520729.1:p.Phe317=
XR_932805.1:n.2460C=
XM_011522424.3:c.2439C=	XP_011520726.1:p.Phe813=
XM_017023043.2:c.1512C=	XP_016878532.1:p.Phe504=
NM_005236.3:c.2301C= MANE Select	NP_005227.1:p.Phe767=