Canonical Allele Identifier: CA2209082862

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948096G= , CM000678.2:g.13948096G=	GRCh38
NC_000016.9:g.14041953G= , CM000678.1:g.14041953G=	GRCh37
NC_000016.8:g.13949454G=	NCBI36
NG_011442.1:g.32940G= , LRG_463:g.32940G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682617.1:c.2638G=	ENSP00000507912.1:p.Asp880=
ENST00000683962.1:c.*2194G=	ENSP00000506854.1:n.*2194G=
ENST00000311895.8:c.2500G= MANE Select	ENSP00000310520.7:p.Asp834=
ENST00000311895.7:c.2500G=	ENSP00000310520.7:p.Asp834=
ENST00000389138.7:n.1777G=
NM_005236.2:c.2500G= , LRG_463t1:c.2500G=	NP_005227.1:p.Asp834=
XM_011522424.1:c.2638G=	XP_011520726.1:p.Asp880=
XM_011522425.1:c.1957G=	XP_011520727.1:p.Asp653=
XM_011522426.1:c.1711G=	XP_011520728.1:p.Asp571=
XM_011522427.1:c.1150G=	XP_011520729.1:p.Asp384=
XR_932805.1:n.2659G=
XM_011522424.3:c.2638G=	XP_011520726.1:p.Asp880=
XM_017023043.2:c.1711G=	XP_016878532.1:p.Asp571=
NM_005236.3:c.2500G= MANE Select	NP_005227.1:p.Asp834=