Canonical Allele Identifier: CA344857019

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830527A>T (hg19) ; chr1:g.214657184A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657184A>T , CM000663.2:g.214657184A>T	GRCh38
NC_000001.10:g.214830527A>T , CM000663.1:g.214830527A>T	GRCh37
NC_000001.9:g.212897150A>T	NCBI36
NG_046787.1:g.59006A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706765.1:c.8560A>T	ENSP00000516538.1:p.Ile2854Phe
ENST00000706766.1:n.836A>T
ENST00000366955.8:c.8737A>T MANE Select	ENSP00000355922.3:p.Ile2913Phe
ENST00000366955.7:c.8737A>T	ENSP00000355922.3:p.Ile2913Phe
ENST00000469862.1:n.508A>T
NM_016343.3:c.8737A>T	NP_057427.3:p.Ile2913Phe
XM_011509082.1:c.8560A>T	XP_011507384.1:p.Ile2854Phe
XM_011509083.1:c.7672A>T	XP_011507385.1:p.Ile2558Phe
XM_011509082.3:c.8560A>T	XP_011507384.1:p.Ile2854Phe
XM_017000086.2:c.8737A>T	XP_016855575.1:p.Ile2913Phe
NM_016343.4:c.8737A>T MANE Select	NP_057427.3:p.Ile2913Phe