Canonical Allele Identifier: CA2067835486
Gene: ANAPC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121318385_121318388delinsGGAA , CM000674.2:g.121318385_121318388delinsGGAA GRCh38
NC_000012.11:g.121756188_121756191delinsGGAA , CM000674.1:g.121756188_121756191delinsGGAA GRCh37
NC_000012.10:g.120240571_120240574delinsGGAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261819.8:c.1782_1785delinsTTCC MANE Select ENSP00000261819.3:p.Ser594=
ENST00000261819.7:c.1782_1785delinsTTCC ENSP00000261819.3:p.Ser594=
ENST00000441917.6:c.1446_1449delinsTTCC ENSP00000415061.2:p.Ser482=
ENST00000534976.5:n.2514_2517delinsTTCC
ENST00000535482.1:c.780_783delinsTTCC ENSP00000438754.1:p.Ser260=
ENST00000535641.5:n.1993_1996delinsTTCC
ENST00000539079.5:c.1106_1109delinsTTCC
ENST00000541887.5:c.1743_1746delinsTTCC ENSP00000439875.1:p.Ser581=
ENST00000544314.5:n.900_903delinsTTCC
ENST00000545218.5:n.989-37_989-34delinsTTCC
NM_001137559.1:c.1446_1449delinsTTCC NP_001131031.1:p.Ser482=
NM_016237.4:c.1782_1785delinsTTCC NP_057321.2:p.Ser594=
XM_005253900.2:c.1743_1746delinsTTCC XP_005253957.1:p.Ser581=
XM_006719449.1:c.588_591delinsTTCC XP_006719512.1:p.Ser196=
NM_001330489.1:c.1743_1746delinsTTCC NP_001317418.1:p.Ser581=
XM_017019423.2:c.588_591delinsTTCC XP_016874912.1:p.Ser196=
XM_017019424.2:c.588_591delinsTTCC XP_016874913.1:p.Ser196=
NM_016237.5:c.1782_1785delinsTTCC MANE Select NP_057321.2:p.Ser594=
NM_001330489.2:c.1743_1746delinsTTCC NP_001317418.1:p.Ser581=