Canonical Allele Identifier: CA2067835695

Gene: ANAPC5

Linked Data

• dbSNP Id: rs1902462253

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318507_121318508insGAA , CM000674.2:g.121318507_121318508insGAA	GRCh38
NC_000012.11:g.121756310_121756311insGAA , CM000674.1:g.121756310_121756311insGAA	GRCh37
NC_000012.10:g.120240693_120240694insGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1739_1740insTCT MANE Select	ENSP00000261819.3:p.Val580_Ile581insLeu
ENST00000261819.7:c.1739_1740insTCT	ENSP00000261819.3:p.Val580_Ile581insLeu
ENST00000441917.6:c.1403_1404insTCT	ENSP00000415061.2:p.Val468_Ile469insLeu
ENST00000534976.5:n.2395_2396insTCT
ENST00000535482.1:c.737_738insTCT	ENSP00000438754.1:p.Val246_Ile247insLeu
ENST00000535641.5:n.1950_1951insTCT
ENST00000539079.5:c.1083_1084insTCT
ENST00000541887.5:c.1700_1701insTCT	ENSP00000439875.1:p.Val567_Ile568insLeu
ENST00000544314.5:n.857_858insTCT
ENST00000545218.5:n.982_983insTCT
NM_001137559.1:c.1403_1404insTCT	NP_001131031.1:p.Val468_Ile469insLeu
NM_016237.4:c.1739_1740insTCT	NP_057321.2:p.Val580_Ile581insLeu
XM_005253900.2:c.1700_1701insTCT	XP_005253957.1:p.Val567_Ile568insLeu
XM_006719449.1:c.545_546insTCT	XP_006719512.1:p.Val182_Ile183insLeu
NM_001330489.1:c.1700_1701insTCT	NP_001317418.1:p.Val567_Ile568insLeu
XM_017019423.2:c.545_546insTCT	XP_016874912.1:p.Val182_Ile183insLeu
XM_017019424.2:c.545_546insTCT	XP_016874913.1:p.Val182_Ile183insLeu
NM_016237.5:c.1739_1740insTCT MANE Select	NP_057321.2:p.Val580_Ile581insLeu
NM_001330489.2:c.1700_1701insTCT	NP_001317418.1:p.Val567_Ile568insLeu