Canonical Allele Identifier: CA2209081400
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13944725A= , CM000678.2:g.13944725A= GRCh38
NC_000016.9:g.14038582A= , CM000678.1:g.14038582A= GRCh37
NC_000016.8:g.13946083A= NCBI36
NG_011442.1:g.29569A= , LRG_463:g.29569A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2045A= ENSP00000507912.1:p.Glu682=
ENST00000683962.1:c.*1601A= ENSP00000506854.1:n.*1601A=
ENST00000311895.8:c.1907A= MANE Select ENSP00000310520.7:p.Glu636=
ENST00000311895.7:c.1907A= ENSP00000310520.7:p.Glu636=
ENST00000389138.7:n.1184A=
ENST00000462862.1:c.220A= ENSP00000461322.1:n.220A=
NM_005236.2:c.1907A= , LRG_463t1:c.1907A= NP_005227.1:p.Glu636=
XM_011522424.1:c.2045A= XP_011520726.1:p.Glu682=
XM_011522425.1:c.1364A= XP_011520727.1:p.Glu455=
XM_011522426.1:c.1118A= XP_011520728.1:p.Glu373=
XM_011522427.1:c.557A= XP_011520729.1:p.Glu186=
XR_932805.1:n.2066A=
XM_011522424.3:c.2045A= XP_011520726.1:p.Glu682=
XM_017023043.2:c.1118A= XP_016878532.1:p.Glu373=
NM_005236.3:c.1907A= MANE Select NP_005227.1:p.Glu636=