Canonical Allele Identifier: CA357778993

Gene: CENPE

Linked Data

• MyVariant Identifiers: chr4:g.104066273T>A (hg19) ; chr4:g.103145116T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.103145116T>A , CM000666.2:g.103145116T>A	GRCh38
NC_000004.11:g.104066273T>A , CM000666.1:g.104066273T>A	GRCh37
NC_000004.10:g.104285722T>A	NCBI36
NG_041798.1:g.58294A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265148.9:c.4791A>T MANE Select	ENSP00000265148.3:p.Arg1597Ser
ENST00000380026.8:c.4716A>T	ENSP00000369365.3:p.Arg1572Ser
ENST00000265148.7:c.4791A>T	ENSP00000265148.3:p.Arg1597Ser
ENST00000380026.7:c.4716A>T	ENSP00000369365.3:p.Arg1572Ser
ENST00000611174.4:c.4791A>T	ENSP00000483542.1:p.Arg1597Ser
NM_001286734.1:c.4716A>T	NP_001273663.1:p.Arg1572Ser
NM_001813.2:c.4791A>T	NP_001804.2:p.Arg1597Ser
XM_011531544.1:c.4716A>T	XP_011529846.1:p.Arg1572Ser
XM_011531545.1:c.4791A>T	XP_011529847.1:p.Arg1597Ser
XM_011531546.1:c.4587A>T	XP_011529848.1:p.Arg1529Ser
XM_011531547.1:c.4791A>T	XP_011529849.1:p.Arg1597Ser
XM_011531548.1:c.4791A>T	XP_011529850.1:p.Arg1597Ser
XM_011531549.1:c.4414-498A>T	XP_011529851.1:n.4414-498A>T
XM_011531544.2:c.4716A>T	XP_011529846.1:p.Arg1572Ser
XM_011531545.2:c.4791A>T	XP_011529847.1:p.Arg1597Ser
XM_011531546.3:c.4587A>T	XP_011529848.1:p.Arg1529Ser
XM_011531547.2:c.4791A>T	XP_011529849.1:p.Arg1597Ser
XM_011531548.2:c.4791A>T	XP_011529850.1:p.Arg1597Ser
XM_011531549.2:c.4414-498A>T	XP_011529851.1:n.4414-498A>T
XM_017007659.1:c.4791A>T	XP_016863148.1:p.Arg1597Ser
NM_001286734.2:c.4716A>T	NP_001273663.1:p.Arg1572Ser
NM_001813.3:c.4791A>T MANE Select	NP_001804.2:p.Arg1597Ser