Canonical Allele Identifier: CA2738203354

Gene: CENPM

Linked Data

• dbSNP Id: rs2146608958

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41942095_41942096del , CM000684.2:g.41942095_41942096del	GRCh38
NC_000022.10:g.42338099_42338100del , CM000684.1:g.42338099_42338100del	GRCh37
NC_000022.9:g.40668045_40668046del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215980.10:c.402+1515_402+1516del MANE Select	ENSP00000215980.5:n.402+1515_402+1516del
ENST00000215980.9:c.402+1515_402+1516del	ENSP00000215980.5:n.402+1515_402+1516del
ENST00000402338.5:c.300+1515_300+1516del	ENSP00000384731.1:n.300+1515_300+1516del
ENST00000402420.1:c.*7+1515_*7+1516del	ENSP00000384132.1:n.*7+1515_*7+1516del
ENST00000404067.5:c.209-2899_209-2898del	ENSP00000384814.1:n.209-2899_209-2898del
ENST00000407253.7:c.311-2899_311-2898del	ENSP00000384743.3:n.311-2899_311-2898del
NM_001002876.2:c.311-2899_311-2898del	NP_001002876.1:n.311-2899_311-2898del
NM_001304370.1:c.300+1515_300+1516del	NP_001291299.1:n.300+1515_300+1516del
NM_001304372.1:c.*7+1515_*7+1516del	NP_001291301.1:n.*7+1515_*7+1516del
NM_001304373.1:c.209-2899_209-2898del	NP_001291302.1:n.209-2899_209-2898del
NM_024053.4:c.402+1515_402+1516del	NP_076958.1:n.402+1515_402+1516del
XM_011530368.1:c.402+1515_402+1516del	XP_011528670.1:n.402+1515_402+1516del
XM_011530368.2:c.402+1515_402+1516del	XP_011528670.1:n.402+1515_402+1516del
NM_024053.5:c.402+1515_402+1516del MANE Select	NP_076958.1:n.402+1515_402+1516del
NM_001002876.3:c.311-2899_311-2898del	NP_001002876.1:n.311-2899_311-2898del
NM_001304370.2:c.300+1515_300+1516del	NP_001291299.1:n.300+1515_300+1516del
NM_001304372.2:c.*7+1515_*7+1516del	NP_001291301.1:n.*7+1515_*7+1516del
NM_001304373.2:c.209-2899_209-2898del	NP_001291302.1:n.209-2899_209-2898del