Canonical Allele Identifier: CA2209083077

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948541C= , CM000678.2:g.13948541C=	GRCh38
NC_000016.9:g.14042398C= , CM000678.1:g.14042398C=	GRCh37
NC_000016.8:g.13949899C=	NCBI36
NG_011442.1:g.33385C= , LRG_463:g.33385C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.*194C=	ENSP00000507912.1:n.*194C=
ENST00000683962.1:c.*2639C=	ENSP00000506854.1:n.*2639C=
ENST00000311895.8:c.*194C= MANE Select	ENSP00000310520.7:n.*194C=
ENST00000311895.7:c.*194C=	ENSP00000310520.7:n.*194C=
NM_005236.2:c.*194C= , LRG_463t1:c.*194C=	NP_005227.1:n.*194C=
XM_011522424.1:c.*194C=	XP_011520726.1:n.*194C=
XM_011522425.1:c.*194C=	XP_011520727.1:n.*194C=
XM_011522426.1:c.*194C=	XP_011520728.1:n.*194C=
XM_011522427.1:c.*194C=	XP_011520729.1:n.*194C=
XR_932805.1:n.3073+31C=
XM_011522424.3:c.*194C=	XP_011520726.1:n.*194C=
XM_017023043.2:c.*194C=	XP_016878532.1:n.*194C=
NM_005236.3:c.*194C= MANE Select	NP_005227.1:n.*194C=