Canonical Allele Identifier: CA2209081433

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944800C= , CM000678.2:g.13944800C=	GRCh38
NC_000016.9:g.14038657C= , CM000678.1:g.14038657C=	GRCh37
NC_000016.8:g.13946158C=	NCBI36
NG_011442.1:g.29644C= , LRG_463:g.29644C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2120C=	ENSP00000507912.1:p.Ala707=
ENST00000683962.1:c.*1676C=	ENSP00000506854.1:n.*1676C=
ENST00000311895.8:c.1982C= MANE Select	ENSP00000310520.7:p.Ala661=
ENST00000311895.7:c.1982C=	ENSP00000310520.7:p.Ala661=
ENST00000389138.7:n.1259C=
ENST00000462862.1:c.295C=	ENSP00000461322.1:n.295C=
NM_005236.2:c.1982C= , LRG_463t1:c.1982C=	NP_005227.1:p.Ala661=
XM_011522424.1:c.2120C=	XP_011520726.1:p.Ala707=
XM_011522425.1:c.1439C=	XP_011520727.1:p.Ala480=
XM_011522426.1:c.1193C=	XP_011520728.1:p.Ala398=
XM_011522427.1:c.632C=	XP_011520729.1:p.Ala211=
XR_932805.1:n.2141C=
XM_011522424.3:c.2120C=	XP_011520726.1:p.Ala707=
XM_017023043.2:c.1193C=	XP_016878532.1:p.Ala398=
NM_005236.3:c.1982C= MANE Select	NP_005227.1:p.Ala661=