Canonical Allele Identifier: CA2486364209
Gene: CENPF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214622139A= , CM000663.2:g.214622139A= GRCh38
NC_000001.10:g.214795482A= , CM000663.1:g.214795482A= GRCh37
NC_000001.9:g.212862105A= NCBI36
NG_046787.1:g.23961A=

Transcript Alleles

HGVS Amino-acid change
ENST00000706764.1:n.1104A=
ENST00000706765.1:c.926A= ENSP00000516538.1:p.Lys309=
ENST00000366955.8:c.926A= MANE Select ENSP00000355922.3:p.Lys309=
ENST00000366955.7:c.926A= ENSP00000355922.3:p.Lys309=
NM_016343.3:c.926A= NP_057427.3:p.Lys309=
XM_011509082.1:c.926A= XP_011507384.1:p.Lys309=
XM_011509082.3:c.926A= XP_011507384.1:p.Lys309=
XM_017000086.2:c.926A= XP_016855575.1:p.Lys309=
NM_016343.4:c.926A= MANE Select NP_057427.3:p.Lys309=