Canonical Allele Identifier: CA2209082713

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947786T= , CM000678.2:g.13947786T=	GRCh38
NC_000016.9:g.14041643T= , CM000678.1:g.14041643T=	GRCh37
NC_000016.8:g.13949144T=	NCBI36
NG_011442.1:g.32630T= , LRG_463:g.32630T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2328T=	ENSP00000507912.1:p.Ser776=
ENST00000683962.1:c.*1884T=	ENSP00000506854.1:n.*1884T=
ENST00000311895.8:c.2190T= MANE Select	ENSP00000310520.7:p.Ser730=
ENST00000311895.7:c.2190T=	ENSP00000310520.7:p.Ser730=
ENST00000389138.7:n.1467T=
ENST00000462862.1:c.503T=	ENSP00000461322.1:n.503T=
NM_005236.2:c.2190T= , LRG_463t1:c.2190T=	NP_005227.1:p.Ser730=
XM_011522424.1:c.2328T=	XP_011520726.1:p.Ser776=
XM_011522425.1:c.1647T=	XP_011520727.1:p.Ser549=
XM_011522426.1:c.1401T=	XP_011520728.1:p.Ser467=
XM_011522427.1:c.840T=	XP_011520729.1:p.Ser280=
XR_932805.1:n.2349T=
XM_011522424.3:c.2328T=	XP_011520726.1:p.Ser776=
XM_017023043.2:c.1401T=	XP_016878532.1:p.Ser467=
NM_005236.3:c.2190T= MANE Select	NP_005227.1:p.Ser730=