Canonical Allele Identifier: CA2209073424

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935660A= , CM000678.2:g.13935660A=	GRCh38
NC_000016.9:g.14029517A= , CM000678.1:g.14029517A=	GRCh37
NC_000016.8:g.13937018A=	NCBI36
NG_011442.1:g.20504A= , LRG_463:g.20504A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1806A=
ENST00000682617.1:c.1866A=	ENSP00000507912.1:p.Arg622=
ENST00000682826.1:c.*1042A=	ENSP00000507274.1:n.*1042A=
ENST00000682909.1:n.3768A=
ENST00000683277.1:n.3373A=
ENST00000683407.1:n.1736A=
ENST00000683962.1:c.*1422A=	ENSP00000506854.1:n.*1422A=
ENST00000311895.8:c.1728A= MANE Select	ENSP00000310520.7:p.Arg576=
ENST00000311895.7:c.1728A=	ENSP00000310520.7:p.Arg576=
ENST00000389138.7:n.1005A=
NM_005236.2:c.1728A= , LRG_463t1:c.1728A=	NP_005227.1:p.Arg576=
XM_011522424.1:c.1866A=	XP_011520726.1:p.Arg622=
XM_011522425.1:c.1185A=	XP_011520727.1:p.Arg395=
XM_011522426.1:c.939A=	XP_011520728.1:p.Arg313=
XM_011522427.1:c.378A=	XP_011520729.1:p.Arg126=
XR_932805.1:n.1887A=
XM_011522424.3:c.1866A=	XP_011520726.1:p.Arg622=
XM_017023043.2:c.939A=	XP_016878532.1:p.Arg313=
NM_005236.3:c.1728A= MANE Select	NP_005227.1:p.Arg576=