Canonical Allele Identifier: CA2406493129

Gene: CENPM

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41942190G= , CM000684.2:g.41942190G=	GRCh38
NC_000022.10:g.42338194G= , CM000684.1:g.42338194G=	GRCh37
NC_000022.9:g.40668140G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215980.10:c.402+1420C= MANE Select	ENSP00000215980.5:n.402+1420C=
ENST00000215980.9:c.402+1420C=	ENSP00000215980.5:n.402+1420C=
ENST00000402338.5:c.300+1420C=	ENSP00000384731.1:n.300+1420C=
ENST00000402420.1:c.*7+1420C=	ENSP00000384132.1:n.*7+1420C=
ENST00000404067.5:c.209-2994C=	ENSP00000384814.1:n.209-2994C=
ENST00000407253.7:c.311-2994C=	ENSP00000384743.3:n.311-2994C=
NM_001002876.2:c.311-2994C=	NP_001002876.1:n.311-2994C=
NM_001304370.1:c.300+1420C=	NP_001291299.1:n.300+1420C=
NM_001304372.1:c.*7+1420C=	NP_001291301.1:n.*7+1420C=
NM_001304373.1:c.209-2994C=	NP_001291302.1:n.209-2994C=
NM_024053.4:c.402+1420C=	NP_076958.1:n.402+1420C=
XM_011530368.1:c.402+1420C=	XP_011528670.1:n.402+1420C=
XM_011530368.2:c.402+1420C=	XP_011528670.1:n.402+1420C=
NM_024053.5:c.402+1420C= MANE Select	NP_076958.1:n.402+1420C=
NM_001002876.3:c.311-2994C=	NP_001002876.1:n.311-2994C=
NM_001304370.2:c.300+1420C=	NP_001291299.1:n.300+1420C=
NM_001304372.2:c.*7+1420C=	NP_001291301.1:n.*7+1420C=
NM_001304373.2:c.209-2994C=	NP_001291302.1:n.209-2994C=