Canonical Allele Identifier: CA2209073536

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935707A= , CM000678.2:g.13935707A=	GRCh38
NC_000016.9:g.14029564A= , CM000678.1:g.14029564A=	GRCh37
NC_000016.8:g.13937065A=	NCBI36
NG_011442.1:g.20551A= , LRG_463:g.20551A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1853A=
ENST00000682617.1:c.1913A=	ENSP00000507912.1:p.Glu638=
ENST00000682826.1:c.*1089A=	ENSP00000507274.1:n.*1089A=
ENST00000682909.1:n.3815A=
ENST00000683277.1:n.3420A=
ENST00000683407.1:n.1783A=
ENST00000683962.1:c.*1469A=	ENSP00000506854.1:n.*1469A=
ENST00000311895.8:c.1775A= MANE Select	ENSP00000310520.7:p.Glu592=
ENST00000311895.7:c.1775A=	ENSP00000310520.7:p.Glu592=
ENST00000389138.7:n.1052A=
NM_005236.2:c.1775A= , LRG_463t1:c.1775A=	NP_005227.1:p.Glu592=
XM_011522424.1:c.1913A=	XP_011520726.1:p.Glu638=
XM_011522425.1:c.1232A=	XP_011520727.1:p.Glu411=
XM_011522426.1:c.986A=	XP_011520728.1:p.Glu329=
XM_011522427.1:c.425A=	XP_011520729.1:p.Glu142=
XR_932805.1:n.1934A=
XM_011522424.3:c.1913A=	XP_011520726.1:p.Glu638=
XM_017023043.2:c.986A=	XP_016878532.1:p.Glu329=
NM_005236.3:c.1775A= MANE Select	NP_005227.1:p.Glu592=