Canonical Allele Identifier: CA2067835686

Gene: ANAPC5

Linked Data

• dbSNP Id: rs1902462162

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318505_121318506del , CM000674.2:g.121318505_121318506del	GRCh38
NC_000012.11:g.121756308_121756309del , CM000674.1:g.121756308_121756309del	GRCh37
NC_000012.10:g.120240691_120240692del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1740_1741del MANE Select	ENSP00000261819.3:p.Ile581GlnfsTer?
ENST00000261819.7:c.1740_1741del	ENSP00000261819.3:p.Ile581GlnfsTer?
ENST00000441917.6:c.1404_1405del	ENSP00000415061.2:p.Ile469GlnfsTer?
ENST00000534976.5:n.2396_2397del
ENST00000535482.1:c.738_739del	ENSP00000438754.1:p.Ile247GlnfsTer?
ENST00000535641.5:n.1951_1952del
ENST00000539079.5:c.1084_1085del
ENST00000541887.5:c.1701_1702del	ENSP00000439875.1:p.Ile568GlnfsTer?
ENST00000544314.5:n.858_859del
ENST00000545218.5:n.983_984del
NM_001137559.1:c.1404_1405del	NP_001131031.1:p.Ile469GlnfsTer?
NM_016237.4:c.1740_1741del	NP_057321.2:p.Ile581GlnfsTer?
XM_005253900.2:c.1701_1702del	XP_005253957.1:p.Ile568GlnfsTer?
XM_006719449.1:c.546_547del	XP_006719512.1:p.Ile183GlnfsTer?
NM_001330489.1:c.1701_1702del	NP_001317418.1:p.Ile568GlnfsTer?
XM_017019423.2:c.546_547del	XP_016874912.1:p.Ile183GlnfsTer?
XM_017019424.2:c.546_547del	XP_016874913.1:p.Ile183GlnfsTer?
NM_016237.5:c.1740_1741del MANE Select	NP_057321.2:p.Ile581GlnfsTer?
NM_001330489.2:c.1701_1702del	NP_001317418.1:p.Ile568GlnfsTer?