Canonical Allele Identifier: CA2209073266

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935565G= , CM000678.2:g.13935565G=	GRCh38
NC_000016.9:g.14029422G= , CM000678.1:g.14029422G=	GRCh37
NC_000016.8:g.13936923G=	NCBI36
NG_011442.1:g.20409G= , LRG_463:g.20409G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682568.1:n.1711G=
ENST00000682617.1:c.1771G=	ENSP00000507912.1:p.Gly591=
ENST00000682826.1:c.*947G=	ENSP00000507274.1:n.*947G=
ENST00000682909.1:n.3673G=
ENST00000683277.1:n.3278G=
ENST00000683407.1:n.1641G=
ENST00000683962.1:c.*1327G=	ENSP00000506854.1:n.*1327G=
ENST00000311895.8:c.1633G= MANE Select	ENSP00000310520.7:p.Gly545=
ENST00000311895.7:c.1633G=	ENSP00000310520.7:p.Gly545=
ENST00000389138.7:n.910G=
NM_005236.2:c.1633G= , LRG_463t1:c.1633G=	NP_005227.1:p.Gly545=
XM_011522424.1:c.1771G=	XP_011520726.1:p.Gly591=
XM_011522425.1:c.1090G=	XP_011520727.1:p.Gly364=
XM_011522426.1:c.844G=	XP_011520728.1:p.Gly282=
XM_011522427.1:c.283G=	XP_011520729.1:p.Gly95=
XR_932805.1:n.1792G=
XM_011522424.3:c.1771G=	XP_011520726.1:p.Gly591=
XM_017023043.2:c.844G=	XP_016878532.1:p.Gly282=
NM_005236.3:c.1633G= MANE Select	NP_005227.1:p.Gly545=