Canonical Allele Identifier: CA11181180

Gene: CENPO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24813989C>A , CM000664.2:g.24813989C>A	GRCh38
NC_000002.11:g.25036858C>A , CM000664.1:g.25036858C>A	GRCh37
NC_000002.10:g.24890362C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380834.7:c.217-387C>A MANE Select	ENSP00000370214.2:n.217-387C>A
ENST00000260662.2:c.217-387C>A	ENSP00000260662.1:n.217-387C>A
ENST00000380834.6:c.217-387C>A	ENSP00000370214.2:n.217-387C>A
ENST00000473706.5:c.199-387C>A	ENSP00000417787.1:n.199-387C>A
ENST00000486527.6:n.342-387C>A
ENST00000491031.5:n.387-387C>A
ENST00000498362.1:n.195-387C>A
NM_001199803.1:c.199-387C>A	NP_001186732.1:n.199-387C>A
NM_024322.2:c.217-387C>A	NP_077298.1:n.217-387C>A
XM_006712102.2:c.217-387C>A	XP_006712165.1:n.217-387C>A
XR_244957.1:n.481-387C>A
XR_244958.1:n.246-387C>A
NM_001199803.2:c.199-387C>A	NP_001186732.1:n.199-387C>A
NM_001322101.1:c.217-387C>A	NP_001309030.1:n.217-387C>A
NM_024322.3:c.217-387C>A	NP_077298.1:n.217-387C>A
NR_136182.1:n.577-387C>A
NR_136183.1:n.577-387C>A
NR_136184.1:n.558-387C>A
XR_244957.2:n.448-387C>A
NM_001322101.2:c.217-387C>A MANE Select	NP_001309030.1:n.217-387C>A
NM_001199803.3:c.199-387C>A	NP_001186732.1:n.199-387C>A
NR_136182.2:n.267-387C>A
NR_136183.2:n.267-387C>A
NR_136184.2:n.248-387C>A
NM_024322.4:c.217-387C>A	NP_077298.1:n.217-387C>A