Canonical Allele Identifier: CA1025929803

Gene: CENPM

Linked Data

• dbSNP Id: rs2077744637
• gnomAD v3: 22-41942057-A-T
• gnomAD v4: 22-41942057-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41942057A>T , CM000684.2:g.41942057A>T	GRCh38
NC_000022.10:g.42338061A>T , CM000684.1:g.42338061A>T	GRCh37
NC_000022.9:g.40668007A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215980.10:c.402+1553T>A MANE Select	ENSP00000215980.5:n.402+1553T>A
ENST00000215980.9:c.402+1553T>A	ENSP00000215980.5:n.402+1553T>A
ENST00000402338.5:c.300+1553T>A	ENSP00000384731.1:n.300+1553T>A
ENST00000402420.1:c.*7+1553T>A	ENSP00000384132.1:n.*7+1553T>A
ENST00000404067.5:c.209-2861T>A	ENSP00000384814.1:n.209-2861T>A
ENST00000407253.7:c.311-2861T>A	ENSP00000384743.3:n.311-2861T>A
NM_001002876.2:c.311-2861T>A	NP_001002876.1:n.311-2861T>A
NM_001304370.1:c.300+1553T>A	NP_001291299.1:n.300+1553T>A
NM_001304372.1:c.*7+1553T>A	NP_001291301.1:n.*7+1553T>A
NM_001304373.1:c.209-2861T>A	NP_001291302.1:n.209-2861T>A
NM_024053.4:c.402+1553T>A	NP_076958.1:n.402+1553T>A
XM_011530368.1:c.402+1553T>A	XP_011528670.1:n.402+1553T>A
XM_011530368.2:c.402+1553T>A	XP_011528670.1:n.402+1553T>A
NM_024053.5:c.402+1553T>A MANE Select	NP_076958.1:n.402+1553T>A
NM_001002876.3:c.311-2861T>A	NP_001002876.1:n.311-2861T>A
NM_001304370.2:c.300+1553T>A	NP_001291299.1:n.300+1553T>A
NM_001304372.2:c.*7+1553T>A	NP_001291301.1:n.*7+1553T>A
NM_001304373.2:c.209-2861T>A	NP_001291302.1:n.209-2861T>A