Canonical Allele Identifier: CA2067835825

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318576_121318577delinsAT , CM000674.2:g.121318576_121318577delinsAT	GRCh38
NC_000012.11:g.121756379_121756380delinsAT , CM000674.1:g.121756379_121756380delinsAT	GRCh37
NC_000012.10:g.120240762_120240763delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1669_1670delinsAT MANE Select	ENSP00000261819.3:p.Met557=
ENST00000261819.7:c.1669_1670delinsAT	ENSP00000261819.3:p.Met557=
ENST00000366333.3:n.881_882delinsAT
ENST00000441917.6:c.1333_1334delinsAT	ENSP00000415061.2:p.Met445=
ENST00000534976.5:n.2325_2326delinsAT
ENST00000535482.1:c.667_668delinsAT	ENSP00000438754.1:p.Met223=
ENST00000535641.5:n.1880_1881delinsAT
ENST00000539079.5:c.1013_1014delinsAT
ENST00000541887.5:c.1630_1631delinsAT	ENSP00000439875.1:p.Met544=
ENST00000544314.5:n.787_788delinsAT
ENST00000545218.5:n.912_913delinsAT
NM_001137559.1:c.1333_1334delinsAT	NP_001131031.1:p.Met445=
NM_016237.4:c.1669_1670delinsAT	NP_057321.2:p.Met557=
XM_005253900.2:c.1630_1631delinsAT	XP_005253957.1:p.Met544=
XM_006719449.1:c.475_476delinsAT	XP_006719512.1:p.Met159=
NM_001330489.1:c.1630_1631delinsAT	NP_001317418.1:p.Met544=
XM_017019423.2:c.475_476delinsAT	XP_016874912.1:p.Met159=
XM_017019424.2:c.475_476delinsAT	XP_016874913.1:p.Met159=
NM_016237.5:c.1669_1670delinsAT MANE Select	NP_057321.2:p.Met557=
NM_001330489.2:c.1630_1631delinsAT	NP_001317418.1:p.Met544=