Canonical Allele Identifier: CA2067835797
Gene: ANAPC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121318560_121318561delinsCT , CM000674.2:g.121318560_121318561delinsCT GRCh38
NC_000012.11:g.121756363_121756364delinsCT , CM000674.1:g.121756363_121756364delinsCT GRCh37
NC_000012.10:g.120240746_120240747delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261819.8:c.1685_1686delinsAG MANE Select ENSP00000261819.3:p.Lys562=
ENST00000261819.7:c.1685_1686delinsAG ENSP00000261819.3:p.Lys562=
ENST00000366333.3:n.897_898delinsAG
ENST00000441917.6:c.1349_1350delinsAG ENSP00000415061.2:p.Lys450=
ENST00000534976.5:n.2341_2342delinsAG
ENST00000535482.1:c.683_684delinsAG ENSP00000438754.1:p.Lys228=
ENST00000535641.5:n.1896_1897delinsAG
ENST00000539079.5:c.1029_1030delinsAG
ENST00000541887.5:c.1646_1647delinsAG ENSP00000439875.1:p.Lys549=
ENST00000544314.5:n.803_804delinsAG
ENST00000545218.5:n.928_929delinsAG
NM_001137559.1:c.1349_1350delinsAG NP_001131031.1:p.Lys450=
NM_016237.4:c.1685_1686delinsAG NP_057321.2:p.Lys562=
XM_005253900.2:c.1646_1647delinsAG XP_005253957.1:p.Lys549=
XM_006719449.1:c.491_492delinsAG XP_006719512.1:p.Lys164=
NM_001330489.1:c.1646_1647delinsAG NP_001317418.1:p.Lys549=
XM_017019423.2:c.491_492delinsAG XP_016874912.1:p.Lys164=
XM_017019424.2:c.491_492delinsAG XP_016874913.1:p.Lys164=
NM_016237.5:c.1685_1686delinsAG MANE Select NP_057321.2:p.Lys562=
NM_001330489.2:c.1646_1647delinsAG NP_001317418.1:p.Lys549=