Canonical Allele Identifier: CA2209073091

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935471A= , CM000678.2:g.13935471A=	GRCh38
NC_000016.9:g.14029328A= , CM000678.1:g.14029328A=	GRCh37
NC_000016.8:g.13936829A=	NCBI36
NG_011442.1:g.20315A= , LRG_463:g.20315A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1617A=
ENST00000682617.1:c.1677A=	ENSP00000507912.1:p.Gly559=
ENST00000682826.1:c.*853A=	ENSP00000507274.1:n.*853A=
ENST00000682909.1:n.3579A=
ENST00000683277.1:n.3184A=
ENST00000683407.1:n.1547A=
ENST00000683962.1:c.*1233A=	ENSP00000506854.1:n.*1233A=
ENST00000311895.8:c.1539A= MANE Select	ENSP00000310520.7:p.Gly513=
ENST00000311895.7:c.1539A=	ENSP00000310520.7:p.Gly513=
ENST00000389138.7:n.816A=
NM_005236.2:c.1539A= , LRG_463t1:c.1539A=	NP_005227.1:p.Gly513=
XM_011522424.1:c.1677A=	XP_011520726.1:p.Gly559=
XM_011522425.1:c.996A=	XP_011520727.1:p.Gly332=
XM_011522426.1:c.750A=	XP_011520728.1:p.Gly250=
XM_011522427.1:c.189A=	XP_011520729.1:p.Gly63=
XR_932805.1:n.1698A=
XM_011522424.3:c.1677A=	XP_011520726.1:p.Gly559=
XM_017023043.2:c.750A=	XP_016878532.1:p.Gly250=
NM_005236.3:c.1539A= MANE Select	NP_005227.1:p.Gly513=