Canonical Allele Identifier: CA3029250

Gene: CENPE

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.103123029C>G , CM000666.2:g.103123029C>G	GRCh38
NC_000004.11:g.104044186C>G , CM000666.1:g.104044186C>G	GRCh37
NC_000004.10:g.104263635C>G	NCBI36
NG_041798.1:g.80381G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265148.9:c.6985G>C MANE Select	ENSP00000265148.3:p.Glu2329Gln
ENST00000380026.8:c.6622G>C	ENSP00000369365.3:p.Glu2208Gln
ENST00000265148.7:c.6985G>C	ENSP00000265148.3:p.Glu2329Gln
ENST00000380026.7:c.6622G>C	ENSP00000369365.3:p.Glu2208Gln
ENST00000611174.4:c.6874G>C	ENSP00000483542.1:p.Glu2292Gln
NM_001286734.1:c.6622G>C	NP_001273663.1:p.Glu2208Gln
NM_001813.2:c.6985G>C	NP_001804.2:p.Glu2329Gln
XM_011531544.1:c.6910G>C	XP_011529846.1:p.Glu2304Gln
XM_011531545.1:c.6826G>C	XP_011529847.1:p.Glu2276Gln
XM_011531546.1:c.6781G>C	XP_011529848.1:p.Glu2261Gln
XM_011531547.1:c.6697G>C	XP_011529849.1:p.Glu2233Gln
XM_011531548.1:c.6694G>C	XP_011529850.1:p.Glu2232Gln
XM_011531549.1:c.6541G>C	XP_011529851.1:p.Glu2181Gln
XM_011531544.2:c.6910G>C	XP_011529846.1:p.Glu2304Gln
XM_011531545.2:c.6826G>C	XP_011529847.1:p.Glu2276Gln
XM_011531546.3:c.6781G>C	XP_011529848.1:p.Glu2261Gln
XM_011531547.2:c.6697G>C	XP_011529849.1:p.Glu2233Gln
XM_011531548.2:c.6694G>C	XP_011529850.1:p.Glu2232Gln
XM_011531549.2:c.6541G>C	XP_011529851.1:p.Glu2181Gln
XM_017007659.1:c.6535G>C	XP_016863148.1:p.Glu2179Gln
NM_001286734.2:c.6622G>C	NP_001273663.1:p.Glu2208Gln
NM_001813.3:c.6985G>C MANE Select	NP_001804.2:p.Glu2329Gln