Canonical Allele Identifier: CA2209082804

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947971C= , CM000678.2:g.13947971C=	GRCh38
NC_000016.9:g.14041828C= , CM000678.1:g.14041828C=	GRCh37
NC_000016.8:g.13949329C=	NCBI36
NG_011442.1:g.32815C= , LRG_463:g.32815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2513C=	ENSP00000507912.1:p.Thr838=
ENST00000683962.1:c.*2069C=	ENSP00000506854.1:n.*2069C=
ENST00000311895.8:c.2375C= MANE Select	ENSP00000310520.7:p.Thr792=
ENST00000311895.7:c.2375C=	ENSP00000310520.7:p.Thr792=
ENST00000389138.7:n.1652C=
ENST00000462862.1:c.688C=	ENSP00000461322.1:n.688C=
NM_005236.2:c.2375C= , LRG_463t1:c.2375C=	NP_005227.1:p.Thr792=
XM_011522424.1:c.2513C=	XP_011520726.1:p.Thr838=
XM_011522425.1:c.1832C=	XP_011520727.1:p.Thr611=
XM_011522426.1:c.1586C=	XP_011520728.1:p.Thr529=
XM_011522427.1:c.1025C=	XP_011520729.1:p.Thr342=
XR_932805.1:n.2534C=
XM_011522424.3:c.2513C=	XP_011520726.1:p.Thr838=
XM_017023043.2:c.1586C=	XP_016878532.1:p.Thr529=
NM_005236.3:c.2375C= MANE Select	NP_005227.1:p.Thr792=