Canonical Allele Identifier: CA2209082766

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947895T= , CM000678.2:g.13947895T=	GRCh38
NC_000016.9:g.14041752T= , CM000678.1:g.14041752T=	GRCh37
NC_000016.8:g.13949253T=	NCBI36
NG_011442.1:g.32739T= , LRG_463:g.32739T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2437T=	ENSP00000507912.1:p.Phe813=
ENST00000683962.1:c.*1993T=	ENSP00000506854.1:n.*1993T=
ENST00000311895.8:c.2299T= MANE Select	ENSP00000310520.7:p.Phe767=
ENST00000311895.7:c.2299T=	ENSP00000310520.7:p.Phe767=
ENST00000389138.7:n.1576T=
ENST00000462862.1:c.612T=	ENSP00000461322.1:n.612T=
NM_005236.2:c.2299T= , LRG_463t1:c.2299T=	NP_005227.1:p.Phe767=
XM_011522424.1:c.2437T=	XP_011520726.1:p.Phe813=
XM_011522425.1:c.1756T=	XP_011520727.1:p.Phe586=
XM_011522426.1:c.1510T=	XP_011520728.1:p.Phe504=
XM_011522427.1:c.949T=	XP_011520729.1:p.Phe317=
XR_932805.1:n.2458T=
XM_011522424.3:c.2437T=	XP_011520726.1:p.Phe813=
XM_017023043.2:c.1510T=	XP_016878532.1:p.Phe504=
NM_005236.3:c.2299T= MANE Select	NP_005227.1:p.Phe767=