Canonical Allele Identifier: CA2738203350

Gene: CENPM

Linked Data

• dbSNP Id: rs2146608944

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41942084A>G , CM000684.2:g.41942084A>G	GRCh38
NC_000022.10:g.42338088A>G , CM000684.1:g.42338088A>G	GRCh37
NC_000022.9:g.40668034A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215980.10:c.402+1526T>C MANE Select	ENSP00000215980.5:n.402+1526T>C
ENST00000215980.9:c.402+1526T>C	ENSP00000215980.5:n.402+1526T>C
ENST00000402338.5:c.300+1526T>C	ENSP00000384731.1:n.300+1526T>C
ENST00000402420.1:c.*7+1526T>C	ENSP00000384132.1:n.*7+1526T>C
ENST00000404067.5:c.209-2888T>C	ENSP00000384814.1:n.209-2888T>C
ENST00000407253.7:c.311-2888T>C	ENSP00000384743.3:n.311-2888T>C
NM_001002876.2:c.311-2888T>C	NP_001002876.1:n.311-2888T>C
NM_001304370.1:c.300+1526T>C	NP_001291299.1:n.300+1526T>C
NM_001304372.1:c.*7+1526T>C	NP_001291301.1:n.*7+1526T>C
NM_001304373.1:c.209-2888T>C	NP_001291302.1:n.209-2888T>C
NM_024053.4:c.402+1526T>C	NP_076958.1:n.402+1526T>C
XM_011530368.1:c.402+1526T>C	XP_011528670.1:n.402+1526T>C
XM_011530368.2:c.402+1526T>C	XP_011528670.1:n.402+1526T>C
NM_024053.5:c.402+1526T>C MANE Select	NP_076958.1:n.402+1526T>C
NM_001002876.3:c.311-2888T>C	NP_001002876.1:n.311-2888T>C
NM_001304370.2:c.300+1526T>C	NP_001291299.1:n.300+1526T>C
NM_001304372.2:c.*7+1526T>C	NP_001291301.1:n.*7+1526T>C
NM_001304373.2:c.209-2888T>C	NP_001291302.1:n.209-2888T>C