Canonical Allele Identifier: CA2209082818

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13948002G= , CM000678.2:g.13948002G=	GRCh38
NC_000016.9:g.14041859G= , CM000678.1:g.14041859G=	GRCh37
NC_000016.8:g.13949360G=	NCBI36
NG_011442.1:g.32846G= , LRG_463:g.32846G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2544G=	ENSP00000507912.1:p.Trp848=
ENST00000683962.1:c.*2100G=	ENSP00000506854.1:n.*2100G=
ENST00000311895.8:c.2406G= MANE Select	ENSP00000310520.7:p.Trp802=
ENST00000311895.7:c.2406G=	ENSP00000310520.7:p.Trp802=
ENST00000389138.7:n.1683G=
ENST00000462862.1:c.719G=	ENSP00000461322.1:n.719G=
NM_005236.2:c.2406G= , LRG_463t1:c.2406G=	NP_005227.1:p.Trp802=
XM_011522424.1:c.2544G=	XP_011520726.1:p.Trp848=
XM_011522425.1:c.1863G=	XP_011520727.1:p.Trp621=
XM_011522426.1:c.1617G=	XP_011520728.1:p.Trp539=
XM_011522427.1:c.1056G=	XP_011520729.1:p.Trp352=
XR_932805.1:n.2565G=
XM_011522424.3:c.2544G=	XP_011520726.1:p.Trp848=
XM_017023043.2:c.1617G=	XP_016878532.1:p.Trp539=
NM_005236.3:c.2406G= MANE Select	NP_005227.1:p.Trp802=