Canonical Allele Identifier: CA2209083110

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948615A= , CM000678.2:g.13948615A=	GRCh38
NC_000016.9:g.14042472A= , CM000678.1:g.14042472A=	GRCh37
NC_000016.8:g.13949973A=	NCBI36
NG_011442.1:g.33459A= , LRG_463:g.33459A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*268A=	ENSP00000507912.1:n.*268A=
ENST00000683962.1:c.*2713A=	ENSP00000506854.1:n.*2713A=
ENST00000311895.8:c.*268A= MANE Select	ENSP00000310520.7:n.*268A=
ENST00000311895.7:c.*268A=	ENSP00000310520.7:n.*268A=
NM_005236.2:c.*268A= , LRG_463t1:c.*268A=	NP_005227.1:n.*268A=
XM_011522424.1:c.*268A=	XP_011520726.1:n.*268A=
XM_011522425.1:c.*268A=	XP_011520727.1:n.*268A=
XM_011522426.1:c.*268A=	XP_011520728.1:n.*268A=
XM_011522427.1:c.*268A=	XP_011520729.1:n.*268A=
XR_932805.1:n.3074-98A=
XM_011522424.3:c.*268A=	XP_011520726.1:n.*268A=
XM_017023043.2:c.*268A=	XP_016878532.1:n.*268A=
NM_005236.3:c.*268A= MANE Select	NP_005227.1:n.*268A=