Canonical Allele Identifier: CA2406493065

Gene: CENPM

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41942055_41942056delinsAG , CM000684.2:g.41942055_41942056delinsAG	GRCh38
NC_000022.10:g.42338059_42338060delinsAG , CM000684.1:g.42338059_42338060delinsAG	GRCh37
NC_000022.9:g.40668005_40668006delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215980.10:c.402+1554_402+1555delinsCT MANE Select	ENSP00000215980.5:n.402+1554_402+1555delinsCT
ENST00000215980.9:c.402+1554_402+1555delinsCT	ENSP00000215980.5:n.402+1554_402+1555delinsCT
ENST00000402338.5:c.300+1554_300+1555delinsCT	ENSP00000384731.1:n.300+1554_300+1555delinsCT
ENST00000402420.1:c.*7+1554_*7+1555delinsCT	ENSP00000384132.1:n.*7+1554_*7+1555delinsCT
ENST00000404067.5:c.209-2860_209-2859delinsCT	ENSP00000384814.1:n.209-2860_209-2859delinsCT
ENST00000407253.7:c.311-2860_311-2859delinsCT	ENSP00000384743.3:n.311-2860_311-2859delinsCT
NM_001002876.2:c.311-2860_311-2859delinsCT	NP_001002876.1:n.311-2860_311-2859delinsCT
NM_001304370.1:c.300+1554_300+1555delinsCT	NP_001291299.1:n.300+1554_300+1555delinsCT
NM_001304372.1:c.*7+1554_*7+1555delinsCT	NP_001291301.1:n.*7+1554_*7+1555delinsCT
NM_001304373.1:c.209-2860_209-2859delinsCT	NP_001291302.1:n.209-2860_209-2859delinsCT
NM_024053.4:c.402+1554_402+1555delinsCT	NP_076958.1:n.402+1554_402+1555delinsCT
XM_011530368.1:c.402+1554_402+1555delinsCT	XP_011528670.1:n.402+1554_402+1555delinsCT
XM_011530368.2:c.402+1554_402+1555delinsCT	XP_011528670.1:n.402+1554_402+1555delinsCT
NM_024053.5:c.402+1554_402+1555delinsCT MANE Select	NP_076958.1:n.402+1554_402+1555delinsCT
NM_001002876.3:c.311-2860_311-2859delinsCT	NP_001002876.1:n.311-2860_311-2859delinsCT
NM_001304370.2:c.300+1554_300+1555delinsCT	NP_001291299.1:n.300+1554_300+1555delinsCT
NM_001304372.2:c.*7+1554_*7+1555delinsCT	NP_001291301.1:n.*7+1554_*7+1555delinsCT
NM_001304373.2:c.209-2860_209-2859delinsCT	NP_001291302.1:n.209-2860_209-2859delinsCT