Canonical Allele Identifier: CA1481685017
Gene: CENPE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103147427T= , CM000666.2:g.103147427T= GRCh38
NC_000004.11:g.104068584T= , CM000666.1:g.104068584T= GRCh37
NC_000004.10:g.104288033T= NCBI36
NG_041798.1:g.55983A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265148.9:c.4063A= MANE Select ENSP00000265148.3:p.Lys1355=
ENST00000380026.8:c.3988A= ENSP00000369365.3:p.Lys1330=
ENST00000265148.7:c.4063A= ENSP00000265148.3:p.Lys1355=
ENST00000380026.7:c.3988A= ENSP00000369365.3:p.Lys1330=
ENST00000611174.4:c.4063A= ENSP00000483542.1:p.Lys1355=
NM_001286734.1:c.3988A= NP_001273663.1:p.Lys1330=
NM_001813.2:c.4063A= NP_001804.2:p.Lys1355=
XM_011531544.1:c.3988A= XP_011529846.1:p.Lys1330=
XM_011531545.1:c.4063A= XP_011529847.1:p.Lys1355=
XM_011531546.1:c.3859A= XP_011529848.1:p.Lys1287=
XM_011531547.1:c.4063A= XP_011529849.1:p.Lys1355=
XM_011531548.1:c.4063A= XP_011529850.1:p.Lys1355=
XM_011531549.1:c.4063A= XP_011529851.1:p.Lys1355=
XM_011531544.2:c.3988A= XP_011529846.1:p.Lys1330=
XM_011531545.2:c.4063A= XP_011529847.1:p.Lys1355=
XM_011531546.3:c.3859A= XP_011529848.1:p.Lys1287=
XM_011531547.2:c.4063A= XP_011529849.1:p.Lys1355=
XM_011531548.2:c.4063A= XP_011529850.1:p.Lys1355=
XM_011531549.2:c.4063A= XP_011529851.1:p.Lys1355=
XM_017007659.1:c.4063A= XP_016863148.1:p.Lys1355=
NM_001286734.2:c.3988A= NP_001273663.1:p.Lys1330=
NM_001813.3:c.4063A= MANE Select NP_001804.2:p.Lys1355=