Canonical Allele Identifier: CA2209081424

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13944783C= , CM000678.2:g.13944783C=	GRCh38
NC_000016.9:g.14038640C= , CM000678.1:g.14038640C=	GRCh37
NC_000016.8:g.13946141C=	NCBI36
NG_011442.1:g.29627C= , LRG_463:g.29627C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2103C=	ENSP00000507912.1:p.Asp701=
ENST00000683962.1:c.*1659C=	ENSP00000506854.1:n.*1659C=
ENST00000311895.8:c.1965C= MANE Select	ENSP00000310520.7:p.Asp655=
ENST00000311895.7:c.1965C=	ENSP00000310520.7:p.Asp655=
ENST00000389138.7:n.1242C=
ENST00000462862.1:c.278C=	ENSP00000461322.1:n.278C=
NM_005236.2:c.1965C= , LRG_463t1:c.1965C=	NP_005227.1:p.Asp655=
XM_011522424.1:c.2103C=	XP_011520726.1:p.Asp701=
XM_011522425.1:c.1422C=	XP_011520727.1:p.Asp474=
XM_011522426.1:c.1176C=	XP_011520728.1:p.Asp392=
XM_011522427.1:c.615C=	XP_011520729.1:p.Asp205=
XR_932805.1:n.2124C=
XM_011522424.3:c.2103C=	XP_011520726.1:p.Asp701=
XM_017023043.2:c.1176C=	XP_016878532.1:p.Asp392=
NM_005236.3:c.1965C= MANE Select	NP_005227.1:p.Asp655=