Canonical Allele Identifier: CA2209082722
Gene: ERCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.13947810C= , CM000678.2:g.13947810C= GRCh38
NC_000016.9:g.14041667C= , CM000678.1:g.14041667C= GRCh37
NC_000016.8:g.13949168C= NCBI36
NG_011442.1:g.32654C= , LRG_463:g.32654C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682617.1:c.2352C= ENSP00000507912.1:p.Asn784=
ENST00000683962.1:c.*1908C= ENSP00000506854.1:n.*1908C=
ENST00000311895.8:c.2214C= MANE Select ENSP00000310520.7:p.Asn738=
ENST00000311895.7:c.2214C= ENSP00000310520.7:p.Asn738=
ENST00000389138.7:n.1491C=
ENST00000462862.1:c.527C= ENSP00000461322.1:n.527C=
NM_005236.2:c.2214C= , LRG_463t1:c.2214C= NP_005227.1:p.Asn738=
XM_011522424.1:c.2352C= XP_011520726.1:p.Asn784=
XM_011522425.1:c.1671C= XP_011520727.1:p.Asn557=
XM_011522426.1:c.1425C= XP_011520728.1:p.Asn475=
XM_011522427.1:c.864C= XP_011520729.1:p.Asn288=
XR_932805.1:n.2373C=
XM_011522424.3:c.2352C= XP_011520726.1:p.Asn784=
XM_017023043.2:c.1425C= XP_016878532.1:p.Asn475=
NM_005236.3:c.2214C= MANE Select NP_005227.1:p.Asn738=