Canonical Allele Identifier: CA1481685535

Gene: CENPE

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.103133529A= , CM000666.2:g.103133529A=	GRCh38
NC_000004.11:g.104054686A= , CM000666.1:g.104054686A=	GRCh37
NC_000004.10:g.104274135A=	NCBI36
NG_041798.1:g.69881T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265148.9:c.6720+166T= MANE Select	ENSP00000265148.3:n.6720+166T=
ENST00000380026.8:c.6357+166T=	ENSP00000369365.3:n.6357+166T=
ENST00000265148.7:c.6720+166T=	ENSP00000265148.3:n.6720+166T=
ENST00000380026.7:c.6357+166T=	ENSP00000369365.3:n.6357+166T=
ENST00000611174.4:c.6609+166T=	ENSP00000483542.1:n.6609+166T=
NM_001286734.1:c.6357+166T=	NP_001273663.1:n.6357+166T=
NM_001813.2:c.6720+166T=	NP_001804.2:n.6720+166T=
XM_011531544.1:c.6645+166T=	XP_011529846.1:n.6645+166T=
XM_011531545.1:c.6561+166T=	XP_011529847.1:n.6561+166T=
XM_011531546.1:c.6516+166T=	XP_011529848.1:n.6516+166T=
XM_011531547.1:c.6432+166T=	XP_011529849.1:n.6432+166T=
XM_011531548.1:c.6429+166T=	XP_011529850.1:n.6429+166T=
XM_011531549.1:c.6276+166T=	XP_011529851.1:n.6276+166T=
XM_011531544.2:c.6645+166T=	XP_011529846.1:n.6645+166T=
XM_011531545.2:c.6561+166T=	XP_011529847.1:n.6561+166T=
XM_011531546.3:c.6516+166T=	XP_011529848.1:n.6516+166T=
XM_011531547.2:c.6432+166T=	XP_011529849.1:n.6432+166T=
XM_011531548.2:c.6429+166T=	XP_011529850.1:n.6429+166T=
XM_011531549.2:c.6276+166T=	XP_011529851.1:n.6276+166T=
XM_017007659.1:c.6270+166T=	XP_016863148.1:n.6270+166T=
NM_001286734.2:c.6357+166T=	NP_001273663.1:n.6357+166T=
NM_001813.3:c.6720+166T= MANE Select	NP_001804.2:n.6720+166T=