Canonical Allele Identifier: CA2406492216

Gene: CENPM

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41940168G= , CM000684.2:g.41940168G=	GRCh38
NC_000022.10:g.42336172G= , CM000684.1:g.42336172G=	GRCh37
NC_000022.9:g.40666118G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024053.5:c.403-972C= MANE Select	NP_076958.1:n.403-972C=
ENST00000215980.10:c.403-972C= MANE Select	ENSP00000215980.5:n.403-972C=
NM_001002876.2:c.311-972C=	NP_001002876.1:n.311-972C=
NM_001002876.3:c.311-972C=	NP_001002876.1:n.311-972C=
NM_001110215.2:c.7C=	NP_001103685.1:p.Arg3=
NM_001110215.3:c.7C=	NP_001103685.1:p.Arg3=
NM_001304370.1:c.301-972C=	NP_001291299.1:n.301-972C=
NM_001304370.2:c.301-972C=	NP_001291299.1:n.301-972C=
NM_001304372.1:c.*8-972C=	NP_001291301.1:n.*8-972C=
NM_001304372.2:c.*8-972C=	NP_001291301.1:n.*8-972C=
NM_001304373.1:c.209-972C=	NP_001291302.1:n.209-972C=
NM_001304373.2:c.209-972C=	NP_001291302.1:n.209-972C=
NM_024053.4:c.403-972C=	NP_076958.1:n.403-972C=
ENST00000215980.9:c.403-972C=	ENSP00000215980.5:n.403-972C=
ENST00000402338.5:c.301-972C=	ENSP00000384731.1:n.301-972C=
ENST00000402420.1:c.*8-972C=	ENSP00000384132.1:n.*8-972C=
ENST00000404067.5:c.209-972C=	ENSP00000384814.1:n.209-972C=
ENST00000407253.7:c.311-972C=	ENSP00000384743.3:n.311-972C=
ENST00000472374.6:c.7C=	ENSP00000430624.1:p.Arg3=
XM_011530368.1:c.402+3442C=	XP_011528670.1:n.402+3442C=
XM_011530368.2:c.402+3442C=	XP_011528670.1:n.402+3442C=