Canonical Allele Identifier: CA2209082734

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947831C= , CM000678.2:g.13947831C=	GRCh38
NC_000016.9:g.14041688C= , CM000678.1:g.14041688C=	GRCh37
NC_000016.8:g.13949189C=	NCBI36
NG_011442.1:g.32675C= , LRG_463:g.32675C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2373C=	ENSP00000507912.1:p.Cys791=
ENST00000683962.1:c.*1929C=	ENSP00000506854.1:n.*1929C=
ENST00000311895.8:c.2235C= MANE Select	ENSP00000310520.7:p.Cys745=
ENST00000311895.7:c.2235C=	ENSP00000310520.7:p.Cys745=
ENST00000389138.7:n.1512C=
ENST00000462862.1:c.548C=	ENSP00000461322.1:n.548C=
NM_005236.2:c.2235C= , LRG_463t1:c.2235C=	NP_005227.1:p.Cys745=
XM_011522424.1:c.2373C=	XP_011520726.1:p.Cys791=
XM_011522425.1:c.1692C=	XP_011520727.1:p.Cys564=
XM_011522426.1:c.1446C=	XP_011520728.1:p.Cys482=
XM_011522427.1:c.885C=	XP_011520729.1:p.Cys295=
XR_932805.1:n.2394C=
XM_011522424.3:c.2373C=	XP_011520726.1:p.Cys791=
XM_017023043.2:c.1446C=	XP_016878532.1:p.Cys482=
NM_005236.3:c.2235C= MANE Select	NP_005227.1:p.Cys745=