Canonical Allele Identifier: CA357783704

Gene: CENPE

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.103158691C>G , CM000666.2:g.103158691C>G	GRCh38
NC_000004.11:g.104079848C>G , CM000666.1:g.104079848C>G	GRCh37
NC_000004.10:g.104299297C>G	NCBI36
NG_041798.1:g.44719G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265148.9:c.2797G>C MANE Select	ENSP00000265148.3:p.Asp933His
ENST00000380026.8:c.2722G>C	ENSP00000369365.3:p.Asp908His
ENST00000265148.7:c.2797G>C	ENSP00000265148.3:p.Asp933His
ENST00000380026.7:c.2722G>C	ENSP00000369365.3:p.Asp908His
ENST00000503705.5:c.2797G>C	ENSP00000423981.1:p.Asp933His
ENST00000611174.4:c.2797G>C	ENSP00000483542.1:p.Asp933His
NM_001286734.1:c.2722G>C	NP_001273663.1:p.Asp908His
NM_001813.2:c.2797G>C	NP_001804.2:p.Asp933His
XM_011531544.1:c.2722G>C	XP_011529846.1:p.Asp908His
XM_011531545.1:c.2797G>C	XP_011529847.1:p.Asp933His
XM_011531546.1:c.2797G>C	XP_011529848.1:p.Asp933His
XM_011531547.1:c.2797G>C	XP_011529849.1:p.Asp933His
XM_011531548.1:c.2797G>C	XP_011529850.1:p.Asp933His
XM_011531549.1:c.2797G>C	XP_011529851.1:p.Asp933His
XM_011531544.2:c.2722G>C	XP_011529846.1:p.Asp908His
XM_011531545.2:c.2797G>C	XP_011529847.1:p.Asp933His
XM_011531546.3:c.2797G>C	XP_011529848.1:p.Asp933His
XM_011531547.2:c.2797G>C	XP_011529849.1:p.Asp933His
XM_011531548.2:c.2797G>C	XP_011529850.1:p.Asp933His
XM_011531549.2:c.2797G>C	XP_011529851.1:p.Asp933His
XM_017007659.1:c.2797G>C	XP_016863148.1:p.Asp933His
NM_001286734.2:c.2722G>C	NP_001273663.1:p.Asp908His
NM_001813.3:c.2797G>C MANE Select	NP_001804.2:p.Asp933His