Canonical Allele Identifier: CA344834294
Gene: CENPF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214622247G>A , CM000663.2:g.214622247G>A GRCh38
NC_000001.10:g.214795590G>A , CM000663.1:g.214795590G>A GRCh37
NC_000001.9:g.212862213G>A NCBI36
NG_046787.1:g.24069G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706764.1:n.1212G>A
ENST00000706765.1:c.1034G>A ENSP00000516538.1:p.Arg345Lys
ENST00000366955.8:c.1034G>A MANE Select ENSP00000355922.3:p.Arg345Lys
ENST00000366955.7:c.1034G>A ENSP00000355922.3:p.Arg345Lys
NM_016343.3:c.1034G>A NP_057427.3:p.Arg345Lys
XM_011509082.1:c.1034G>A XP_011507384.1:p.Arg345Lys
XM_011509082.3:c.1034G>A XP_011507384.1:p.Arg345Lys
XM_017000086.2:c.1034G>A XP_016855575.1:p.Arg345Lys
NM_016343.4:c.1034G>A MANE Select NP_057427.3:p.Arg345Lys