Canonical Allele Identifier: CA5124568

Gene: OMD CENPP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92417345A>G , CM000671.2:g.92417345A>G	GRCh38
NC_000009.11:g.95179627A>G , CM000671.1:g.95179627A>G	GRCh37
NC_000009.10:g.94219448A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001012267.3:c.564+37486A>G (CENPP) MANE Select	NP_001012267.1:n.564+37486A>G
NM_005014.3:c.214T>C (OMD) MANE Select	NP_005005.1:p.Phe72Leu
ENST00000375550.5:c.214T>C (OMD) MANE Select	ENSP00000364700.4:p.Phe72Leu
ENST00000375587.8:c.564+37486A>G (CENPP) MANE Select	ENSP00000364737.3:n.564+37486A>G
NM_001012267.2:c.564+37486A>G (CENPP)	NP_001012267.1:n.564+37486A>G
NM_001286969.1:c.228+37486A>G (CENPP)	NP_001273898.1:n.228+37486A>G
NM_005014.2:c.214T>C (OMD)	NP_005005.1:p.Phe72Leu
ENST00000375550.4:c.214T>C (OMD)	ENSP00000364700.4:p.Phe72Leu
ENST00000375587.7:c.564+37486A>G (CENPP)	ENSP00000364737.3:n.564+37486A>G
XM_011518686.1:c.565-1674A>G (CENPP)	XP_011516988.1:n.565-1674A>G
XM_011518687.1:c.565-18282A>G (CENPP)	XP_011516989.1:n.565-18282A>G
XM_011518688.1:c.564+37486A>G (CENPP)	XP_011516990.1:n.564+37486A>G
XM_011518689.1:c.564+37486A>G (CENPP)	XP_011516991.1:n.564+37486A>G
XM_024447543.1:c.288+37486A>G (CENPP)	XP_024303311.1:n.288+37486A>G