Canonical Allele Identifier: CA102732874

Gene: CENPE

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.103146222G>C , CM000666.2:g.103146222G>C	GRCh38
NC_000004.11:g.104067379G>C , CM000666.1:g.104067379G>C	GRCh37
NC_000004.10:g.104286828G>C	NCBI36
NG_041798.1:g.57188C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001813.3:c.4135-115C>G MANE Select	NP_001804.2:n.4135-115C>G
ENST00000265148.9:c.4135-115C>G MANE Select	ENSP00000265148.3:n.4135-115C>G
NM_001286734.1:c.4060-115C>G	NP_001273663.1:n.4060-115C>G
NM_001286734.2:c.4060-115C>G	NP_001273663.1:n.4060-115C>G
NM_001813.2:c.4135-115C>G	NP_001804.2:n.4135-115C>G
ENST00000265148.7:c.4135-115C>G	ENSP00000265148.3:n.4135-115C>G
ENST00000380026.7:c.4060-115C>G	ENSP00000369365.3:n.4060-115C>G
ENST00000380026.8:c.4060-115C>G	ENSP00000369365.3:n.4060-115C>G
ENST00000611174.4:c.4135-115C>G	ENSP00000483542.1:n.4135-115C>G
XM_011531544.1:c.4060-115C>G	XP_011529846.1:n.4060-115C>G
XM_011531544.2:c.4060-115C>G	XP_011529846.1:n.4060-115C>G
XM_011531545.1:c.4135-115C>G	XP_011529847.1:n.4135-115C>G
XM_011531545.2:c.4135-115C>G	XP_011529847.1:n.4135-115C>G
XM_011531546.1:c.3931-115C>G	XP_011529848.1:n.3931-115C>G
XM_011531546.3:c.3931-115C>G	XP_011529848.1:n.3931-115C>G
XM_011531547.1:c.4135-115C>G	XP_011529849.1:n.4135-115C>G
XM_011531547.2:c.4135-115C>G	XP_011529849.1:n.4135-115C>G
XM_011531548.1:c.4135-115C>G	XP_011529850.1:n.4135-115C>G
XM_011531548.2:c.4135-115C>G	XP_011529850.1:n.4135-115C>G
XM_011531549.1:c.4135-115C>G	XP_011529851.1:n.4135-115C>G
XM_011531549.2:c.4135-115C>G	XP_011529851.1:n.4135-115C>G
XM_017007659.1:c.4135-115C>G	XP_016863148.1:n.4135-115C>G