Canonical Allele Identifier: CA2840225139
Gene: CENPF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657300dup , CM000663.2:g.214657300dup GRCh38
NC_000001.10:g.214830643dup , CM000663.1:g.214830643dup GRCh37
NC_000001.9:g.212897266dup NCBI36
NG_046787.1:g.59122dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8676dup ENSP00000516538.1:p.Ser2893GlufsTer4
ENST00000706766.1:n.952dup
ENST00000366955.8:c.8853dup MANE Select ENSP00000355922.3:p.Ser2952GlufsTer4
ENST00000366955.7:c.8853dup ENSP00000355922.3:p.Ser2952GlufsTer4
ENST00000469862.1:n.624dup
NM_016343.3:c.8853dup NP_057427.3:p.Ser2952GlufsTer4
XM_011509082.1:c.8676dup XP_011507384.1:p.Ser2893GlufsTer4
XM_011509083.1:c.7788dup XP_011507385.1:p.Ser2597GlufsTer4
XM_011509082.3:c.8676dup XP_011507384.1:p.Ser2893GlufsTer4
XM_017000086.2:c.8853dup XP_016855575.1:p.Ser2952GlufsTer4
NM_016343.4:c.8853dup MANE Select NP_057427.3:p.Ser2952GlufsTer4