Canonical Allele Identifier: CA2209082735

Gene: ERCC4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.13947832A= , CM000678.2:g.13947832A=	GRCh38
NC_000016.9:g.14041689A= , CM000678.1:g.14041689A=	GRCh37
NC_000016.8:g.13949190A=	NCBI36
NG_011442.1:g.32676A= , LRG_463:g.32676A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682617.1:c.2374A=	ENSP00000507912.1:p.Ile792=
ENST00000683962.1:c.*1930A=	ENSP00000506854.1:n.*1930A=
ENST00000311895.8:c.2236A= MANE Select	ENSP00000310520.7:p.Ile746=
ENST00000311895.7:c.2236A=	ENSP00000310520.7:p.Ile746=
ENST00000389138.7:n.1513A=
ENST00000462862.1:c.549A=	ENSP00000461322.1:n.549A=
NM_005236.2:c.2236A= , LRG_463t1:c.2236A=	NP_005227.1:p.Ile746=
XM_011522424.1:c.2374A=	XP_011520726.1:p.Ile792=
XM_011522425.1:c.1693A=	XP_011520727.1:p.Ile565=
XM_011522426.1:c.1447A=	XP_011520728.1:p.Ile483=
XM_011522427.1:c.886A=	XP_011520729.1:p.Ile296=
XR_932805.1:n.2395A=
XM_011522424.3:c.2374A=	XP_011520726.1:p.Ile792=
XM_017023043.2:c.1447A=	XP_016878532.1:p.Ile483=
NM_005236.3:c.2236A= MANE Select	NP_005227.1:p.Ile746=