Canonical Allele Identifier: CA2209073099

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13935476G= , CM000678.2:g.13935476G=	GRCh38
NC_000016.9:g.14029333G= , CM000678.1:g.14029333G=	GRCh37
NC_000016.8:g.13936834G=	NCBI36
NG_011442.1:g.20320G= , LRG_463:g.20320G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682568.1:n.1622G=
ENST00000682617.1:c.1682G=	ENSP00000507912.1:p.Arg561=
ENST00000682826.1:c.*858G=	ENSP00000507274.1:n.*858G=
ENST00000682909.1:n.3584G=
ENST00000683277.1:n.3189G=
ENST00000683407.1:n.1552G=
ENST00000683962.1:c.*1238G=	ENSP00000506854.1:n.*1238G=
ENST00000311895.8:c.1544G= MANE Select	ENSP00000310520.7:p.Arg515=
ENST00000311895.7:c.1544G=	ENSP00000310520.7:p.Arg515=
ENST00000389138.7:n.821G=
NM_005236.2:c.1544G= , LRG_463t1:c.1544G=	NP_005227.1:p.Arg515=
XM_011522424.1:c.1682G=	XP_011520726.1:p.Arg561=
XM_011522425.1:c.1001G=	XP_011520727.1:p.Arg334=
XM_011522426.1:c.755G=	XP_011520728.1:p.Arg252=
XM_011522427.1:c.194G=	XP_011520729.1:p.Arg65=
XR_932805.1:n.1703G=
XM_011522424.3:c.1682G=	XP_011520726.1:p.Arg561=
XM_017023043.2:c.755G=	XP_016878532.1:p.Arg252=
NM_005236.3:c.1544G= MANE Select	NP_005227.1:p.Arg515=