Canonical Allele Identifier: CA2840225141
Gene: CENPF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657324dup , CM000663.2:g.214657324dup GRCh38
NC_000001.10:g.214830667dup , CM000663.1:g.214830667dup GRCh37
NC_000001.9:g.212897290dup NCBI36
NG_046787.1:g.59146dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8700dup ENSP00000516538.1:p.Ala2901SerfsTer16
ENST00000706766.1:n.976dup
ENST00000366955.8:c.8877dup MANE Select ENSP00000355922.3:p.Ala2960SerfsTer16
ENST00000366955.7:c.8877dup ENSP00000355922.3:p.Ala2960SerfsTer16
ENST00000469862.1:n.648dup
NM_016343.3:c.8877dup NP_057427.3:p.Ala2960SerfsTer16
XM_011509082.1:c.8700dup XP_011507384.1:p.Ala2901SerfsTer16
XM_011509083.1:c.7812dup XP_011507385.1:p.Ala2605SerfsTer16
XM_011509082.3:c.8700dup XP_011507384.1:p.Ala2901SerfsTer16
XM_017000086.2:c.8877dup XP_016855575.1:p.Ala2960SerfsTer16
NM_016343.4:c.8877dup MANE Select NP_057427.3:p.Ala2960SerfsTer16