Canonical Allele Identifier: CA2209082962

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948310T= , CM000678.2:g.13948310T=	GRCh38
NC_000016.9:g.14042167T= , CM000678.1:g.14042167T=	GRCh37
NC_000016.8:g.13949668T=	NCBI36
NG_011442.1:g.33154T= , LRG_463:g.33154T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2852T=	ENSP00000507912.1:p.Phe951=
ENST00000683962.1:c.*2408T=	ENSP00000506854.1:n.*2408T=
ENST00000311895.8:c.2714T= MANE Select	ENSP00000310520.7:p.Phe905=
ENST00000311895.7:c.2714T=	ENSP00000310520.7:p.Phe905=
ENST00000389138.7:n.1991T=
NM_005236.2:c.2714T= , LRG_463t1:c.2714T=	NP_005227.1:p.Phe905=
XM_011522424.1:c.2852T=	XP_011520726.1:p.Phe951=
XM_011522425.1:c.2171T=	XP_011520727.1:p.Phe724=
XM_011522426.1:c.1925T=	XP_011520728.1:p.Phe642=
XM_011522427.1:c.1364T=	XP_011520729.1:p.Phe455=
XR_932805.1:n.2873T=
XM_011522424.3:c.2852T=	XP_011520726.1:p.Phe951=
XM_017023043.2:c.1925T=	XP_016878532.1:p.Phe642=
NM_005236.3:c.2714T= MANE Select	NP_005227.1:p.Phe905=