Canonical Allele Identifier: CA357780748

Gene: CENPE

Linked Data

• MyVariant Identifiers: chr4:g.104068589T>G (hg19) ; chr4:g.103147432T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.103147432T>G , CM000666.2:g.103147432T>G	GRCh38
NC_000004.11:g.104068589T>G , CM000666.1:g.104068589T>G	GRCh37
NC_000004.10:g.104288038T>G	NCBI36
NG_041798.1:g.55978A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265148.9:c.4058A>C MANE Select	ENSP00000265148.3:p.Asn1353Thr
ENST00000380026.8:c.3983A>C	ENSP00000369365.3:p.Asn1328Thr
ENST00000265148.7:c.4058A>C	ENSP00000265148.3:p.Asn1353Thr
ENST00000380026.7:c.3983A>C	ENSP00000369365.3:p.Asn1328Thr
ENST00000611174.4:c.4058A>C	ENSP00000483542.1:p.Asn1353Thr
NM_001286734.1:c.3983A>C	NP_001273663.1:p.Asn1328Thr
NM_001813.2:c.4058A>C	NP_001804.2:p.Asn1353Thr
XM_011531544.1:c.3983A>C	XP_011529846.1:p.Asn1328Thr
XM_011531545.1:c.4058A>C	XP_011529847.1:p.Asn1353Thr
XM_011531546.1:c.3854A>C	XP_011529848.1:p.Asn1285Thr
XM_011531547.1:c.4058A>C	XP_011529849.1:p.Asn1353Thr
XM_011531548.1:c.4058A>C	XP_011529850.1:p.Asn1353Thr
XM_011531549.1:c.4058A>C	XP_011529851.1:p.Asn1353Thr
XM_011531544.2:c.3983A>C	XP_011529846.1:p.Asn1328Thr
XM_011531545.2:c.4058A>C	XP_011529847.1:p.Asn1353Thr
XM_011531546.3:c.3854A>C	XP_011529848.1:p.Asn1285Thr
XM_011531547.2:c.4058A>C	XP_011529849.1:p.Asn1353Thr
XM_011531548.2:c.4058A>C	XP_011529850.1:p.Asn1353Thr
XM_011531549.2:c.4058A>C	XP_011529851.1:p.Asn1353Thr
XM_017007659.1:c.4058A>C	XP_016863148.1:p.Asn1353Thr
NM_001286734.2:c.3983A>C	NP_001273663.1:p.Asn1328Thr
NM_001813.3:c.4058A>C MANE Select	NP_001804.2:p.Asn1353Thr