Canonical Allele Identifier: CA2209082667

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947691A= , CM000678.2:g.13947691A=	GRCh38
NC_000016.9:g.14041548A= , CM000678.1:g.14041548A=	GRCh37
NC_000016.8:g.13949049A=	NCBI36
NG_011442.1:g.32535A= , LRG_463:g.32535A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005236.3:c.2095A= MANE Select	NP_005227.1:p.Ile699=
ENST00000311895.8:c.2095A= MANE Select	ENSP00000310520.7:p.Ile699=
NM_005236.2:c.2095A= , LRG_463t1:c.2095A=	NP_005227.1:p.Ile699=
ENST00000311895.7:c.2095A=	ENSP00000310520.7:p.Ile699=
ENST00000389138.7:n.1372A=
ENST00000462862.1:c.408A=	ENSP00000461322.1:n.408A=
ENST00000682617.1:c.2233A=	ENSP00000507912.1:p.Ile745=
ENST00000683962.1:c.*1789A=	ENSP00000506854.1:n.*1789A=
XM_011522424.1:c.2233A=	XP_011520726.1:p.Ile745=
XM_011522424.3:c.2233A=	XP_011520726.1:p.Ile745=
XM_011522425.1:c.1552A=	XP_011520727.1:p.Ile518=
XM_011522426.1:c.1306A=	XP_011520728.1:p.Ile436=
XM_011522427.1:c.745A=	XP_011520729.1:p.Ile249=
XM_017023043.2:c.1306A=	XP_016878532.1:p.Ile436=
XR_932805.1:n.2254A=