Canonical Allele Identifier: CA2830534854
Gene: CENPE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103161248del , CM000666.2:g.103161248del GRCh38
NC_000004.11:g.104082405del , CM000666.1:g.104082405del GRCh37
NC_000004.10:g.104301854del NCBI36
NG_041798.1:g.42162del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265148.9:c.1969del MANE Select ENSP00000265148.3:p.Glu657AsnfsTer?
ENST00000380026.8:c.1894del ENSP00000369365.3:p.Glu632AsnfsTer?
ENST00000265148.7:c.1969del ENSP00000265148.3:p.Glu657AsnfsTer?
ENST00000380026.7:c.1894del ENSP00000369365.3:p.Glu632AsnfsTer?
ENST00000503705.5:c.1969del ENSP00000423981.1:p.Glu657AsnfsTer?
ENST00000611174.4:c.1969del ENSP00000483542.1:p.Glu657AsnfsTer?
NM_001286734.1:c.1894del NP_001273663.1:p.Glu632AsnfsTer?
NM_001813.2:c.1969del NP_001804.2:p.Glu657AsnfsTer?
XM_011531544.1:c.1894del XP_011529846.1:p.Glu632AsnfsTer?
XM_011531545.1:c.1969del XP_011529847.1:p.Glu657AsnfsTer?
XM_011531546.1:c.1969del XP_011529848.1:p.Glu657AsnfsTer?
XM_011531547.1:c.1969del XP_011529849.1:p.Glu657AsnfsTer?
XM_011531548.1:c.1969del XP_011529850.1:p.Glu657AsnfsTer?
XM_011531549.1:c.1969del XP_011529851.1:p.Glu657AsnfsTer?
XM_011531544.2:c.1894del XP_011529846.1:p.Glu632AsnfsTer?
XM_011531545.2:c.1969del XP_011529847.1:p.Glu657AsnfsTer?
XM_011531546.3:c.1969del XP_011529848.1:p.Glu657AsnfsTer?
XM_011531547.2:c.1969del XP_011529849.1:p.Glu657AsnfsTer?
XM_011531548.2:c.1969del XP_011529850.1:p.Glu657AsnfsTer?
XM_011531549.2:c.1969del XP_011529851.1:p.Glu657AsnfsTer?
XM_017007659.1:c.1969del XP_016863148.1:p.Glu657AsnfsTer?
NM_001286734.2:c.1894del NP_001273663.1:p.Glu632AsnfsTer?
NM_001813.3:c.1969del MANE Select NP_001804.2:p.Glu657AsnfsTer?