Canonical Allele Identifier: CA2209082778

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947913G= , CM000678.2:g.13947913G=	GRCh38
NC_000016.9:g.14041770G= , CM000678.1:g.14041770G=	GRCh37
NC_000016.8:g.13949271G=	NCBI36
NG_011442.1:g.32757G= , LRG_463:g.32757G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2455G=	ENSP00000507912.1:p.Gly819=
ENST00000683962.1:c.*2011G=	ENSP00000506854.1:n.*2011G=
ENST00000311895.8:c.2317G= MANE Select	ENSP00000310520.7:p.Gly773=
ENST00000311895.7:c.2317G=	ENSP00000310520.7:p.Gly773=
ENST00000389138.7:n.1594G=
ENST00000462862.1:c.630G=	ENSP00000461322.1:n.630G=
NM_005236.2:c.2317G= , LRG_463t1:c.2317G=	NP_005227.1:p.Gly773=
XM_011522424.1:c.2455G=	XP_011520726.1:p.Gly819=
XM_011522425.1:c.1774G=	XP_011520727.1:p.Gly592=
XM_011522426.1:c.1528G=	XP_011520728.1:p.Gly510=
XM_011522427.1:c.967G=	XP_011520729.1:p.Gly323=
XR_932805.1:n.2476G=
XM_011522424.3:c.2455G=	XP_011520726.1:p.Gly819=
XM_017023043.2:c.1528G=	XP_016878532.1:p.Gly510=
NM_005236.3:c.2317G= MANE Select	NP_005227.1:p.Gly773=