Canonical Allele Identifier: CA111933253

Gene: CENPU

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.184718015G>C , CM000666.2:g.184718015G>C	GRCh38
NC_000004.11:g.185639169G>C , CM000666.1:g.185639169G>C	GRCh37
NC_000004.10:g.185876163G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281453.10:c.321-819C>G MANE Select	ENSP00000281453.5:n.321-819C>G
ENST00000281453.9:c.321-819C>G	ENSP00000281453.5:n.321-819C>G
ENST00000510146.5:c.321-819C>G	ENSP00000423248.1:n.321-819C>G
ENST00000514781.1:c.234-819C>G	ENSP00000423167.1:n.234-819C>G
NM_024629.3:c.321-819C>G	NP_078905.2:n.321-819C>G
NR_104593.1:n.391-819C>G
XM_005263218.3:c.411-819C>G	XP_005263275.2:n.411-819C>G
XM_005263218.4:c.411-819C>G	XP_005263275.2:n.411-819C>G
NM_024629.4:c.321-819C>G MANE Select	NP_078905.2:n.321-819C>G
NR_104593.2:n.355-819C>G