Canonical Allele Identifier: CA2209082792

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947945C= , CM000678.2:g.13947945C=	GRCh38
NC_000016.9:g.14041802C= , CM000678.1:g.14041802C=	GRCh37
NC_000016.8:g.13949303C=	NCBI36
NG_011442.1:g.32789C= , LRG_463:g.32789C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2487C=	ENSP00000507912.1:p.Asp829=
ENST00000683962.1:c.*2043C=	ENSP00000506854.1:n.*2043C=
ENST00000311895.8:c.2349C= MANE Select	ENSP00000310520.7:p.Asp783=
ENST00000311895.7:c.2349C=	ENSP00000310520.7:p.Asp783=
ENST00000389138.7:n.1626C=
ENST00000462862.1:c.662C=	ENSP00000461322.1:n.662C=
NM_005236.2:c.2349C= , LRG_463t1:c.2349C=	NP_005227.1:p.Asp783=
XM_011522424.1:c.2487C=	XP_011520726.1:p.Asp829=
XM_011522425.1:c.1806C=	XP_011520727.1:p.Asp602=
XM_011522426.1:c.1560C=	XP_011520728.1:p.Asp520=
XM_011522427.1:c.999C=	XP_011520729.1:p.Asp333=
XR_932805.1:n.2508C=
XM_011522424.3:c.2487C=	XP_011520726.1:p.Asp829=
XM_017023043.2:c.1560C=	XP_016878532.1:p.Asp520=
NM_005236.3:c.2349C= MANE Select	NP_005227.1:p.Asp783=