Canonical Allele Identifier: CA2209081438
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13944808G= , CM000678.2:g.13944808G= GRCh38
NC_000016.9:g.14038665G= , CM000678.1:g.14038665G= GRCh37
NC_000016.8:g.13946166G= NCBI36
NG_011442.1:g.29652G= , LRG_463:g.29652G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2128G= ENSP00000507912.1:p.Asp710=
ENST00000683962.1:c.*1684G= ENSP00000506854.1:n.*1684G=
ENST00000311895.8:c.1990G= MANE Select ENSP00000310520.7:p.Asp664=
ENST00000311895.7:c.1990G= ENSP00000310520.7:p.Asp664=
ENST00000389138.7:n.1267G=
ENST00000462862.1:c.303G= ENSP00000461322.1:n.303G=
NM_005236.2:c.1990G= , LRG_463t1:c.1990G= NP_005227.1:p.Asp664=
XM_011522424.1:c.2128G= XP_011520726.1:p.Asp710=
XM_011522425.1:c.1447G= XP_011520727.1:p.Asp483=
XM_011522426.1:c.1201G= XP_011520728.1:p.Asp401=
XM_011522427.1:c.640G= XP_011520729.1:p.Asp214=
XR_932805.1:n.2149G=
XM_011522424.3:c.2128G= XP_011520726.1:p.Asp710=
XM_017023043.2:c.1201G= XP_016878532.1:p.Asp401=
NM_005236.3:c.1990G= MANE Select NP_005227.1:p.Asp664=