Canonical Allele Identifier: CA2209082984

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948350A= , CM000678.2:g.13948350A=	GRCh38
NC_000016.9:g.14042207A= , CM000678.1:g.14042207A=	GRCh37
NC_000016.8:g.13949708A=	NCBI36
NG_011442.1:g.33194A= , LRG_463:g.33194A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*3A=	ENSP00000507912.1:n.*3A=
ENST00000683962.1:c.*2448A=	ENSP00000506854.1:n.*2448A=
ENST00000311895.8:c.*3A= MANE Select	ENSP00000310520.7:n.*3A=
ENST00000311895.7:c.*3A=	ENSP00000310520.7:n.*3A=
ENST00000389138.7:n.2031A=
NM_005236.2:c.*3A= , LRG_463t1:c.*3A=	NP_005227.1:n.*3A=
XM_011522424.1:c.*3A=	XP_011520726.1:n.*3A=
XM_011522425.1:c.*3A=	XP_011520727.1:n.*3A=
XM_011522426.1:c.*3A=	XP_011520728.1:n.*3A=
XM_011522427.1:c.*3A=	XP_011520729.1:n.*3A=
XR_932805.1:n.2913A=
XM_011522424.3:c.*3A=	XP_011520726.1:n.*3A=
XM_017023043.2:c.*3A=	XP_016878532.1:n.*3A=
NM_005236.3:c.*3A= MANE Select	NP_005227.1:n.*3A=