Canonical Allele Identifier: CA2209083114

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948628G= , CM000678.2:g.13948628G=	GRCh38
NC_000016.9:g.14042485G= , CM000678.1:g.14042485G=	GRCh37
NC_000016.8:g.13949986G=	NCBI36
NG_011442.1:g.33472G= , LRG_463:g.33472G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*281G=	ENSP00000507912.1:n.*281G=
ENST00000683962.1:c.*2726G=	ENSP00000506854.1:n.*2726G=
ENST00000311895.8:c.*281G= MANE Select	ENSP00000310520.7:n.*281G=
ENST00000311895.7:c.*281G=	ENSP00000310520.7:n.*281G=
NM_005236.2:c.*281G= , LRG_463t1:c.*281G=	NP_005227.1:n.*281G=
XM_011522424.1:c.*281G=	XP_011520726.1:n.*281G=
XM_011522425.1:c.*281G=	XP_011520727.1:n.*281G=
XM_011522426.1:c.*281G=	XP_011520728.1:n.*281G=
XM_011522427.1:c.*281G=	XP_011520729.1:n.*281G=
XR_932805.1:n.3074-85G=
XM_011522424.3:c.*281G=	XP_011520726.1:n.*281G=
XM_017023043.2:c.*281G=	XP_016878532.1:n.*281G=
NM_005236.3:c.*281G= MANE Select	NP_005227.1:n.*281G=