Canonical Allele Identifier: CA344856860
Gene: CENPF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657103G>A , CM000663.2:g.214657103G>A GRCh38
NC_000001.10:g.214830446G>A , CM000663.1:g.214830446G>A GRCh37
NC_000001.9:g.212897069G>A NCBI36
NG_046787.1:g.58925G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8479G>A ENSP00000516538.1:p.Ala2827Thr
ENST00000706766.1:n.755G>A
ENST00000366955.8:c.8656G>A MANE Select ENSP00000355922.3:p.Ala2886Thr
ENST00000366955.7:c.8656G>A ENSP00000355922.3:p.Ala2886Thr
ENST00000469862.1:n.427G>A
NM_016343.3:c.8656G>A NP_057427.3:p.Ala2886Thr
XM_011509082.1:c.8479G>A XP_011507384.1:p.Ala2827Thr
XM_011509083.1:c.7591G>A XP_011507385.1:p.Ala2531Thr
XM_011509082.3:c.8479G>A XP_011507384.1:p.Ala2827Thr
XM_017000086.2:c.8656G>A XP_016855575.1:p.Ala2886Thr
NM_016343.4:c.8656G>A MANE Select NP_057427.3:p.Ala2886Thr