Canonical Allele Identifier: CA2486377744
Gene: CENPF HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657456C= , CM000663.2:g.214657456C= GRCh38
NC_000001.10:g.214830799C= , CM000663.1:g.214830799C= GRCh37
NC_000001.9:g.212897422C= NCBI36
NG_046787.1:g.59278C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8785+47C= ENSP00000516538.1:n.8785+47C=
ENST00000706766.1:n.1061+47C=
ENST00000366955.8:c.8962+47C= MANE Select ENSP00000355922.3:n.8962+47C=
ENST00000366955.7:c.8962+47C= ENSP00000355922.3:n.8962+47C=
NM_016343.3:c.8962+47C= NP_057427.3:n.8962+47C=
XM_011509082.1:c.8785+47C= XP_011507384.1:n.8785+47C=
XM_011509083.1:c.7897+47C= XP_011507385.1:n.7897+47C=
XM_011509082.3:c.8785+47C= XP_011507384.1:n.8785+47C=
XM_017000086.2:c.8962+47C= XP_016855575.1:n.8962+47C=
NM_016343.4:c.8962+47C= MANE Select NP_057427.3:n.8962+47C=
Search 100 bp 5'
Search 100 bp 3'