Canonical Allele Identifier: CA2840225140
Gene: CENPF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657315_214657316del , CM000663.2:g.214657315_214657316del GRCh38
NC_000001.10:g.214830658_214830659del , CM000663.1:g.214830658_214830659del GRCh37
NC_000001.9:g.212897281_212897282del NCBI36
NG_046787.1:g.59137_59138del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8691_8692del ENSP00000516538.1:p.Ser2898GlnfsTer18
ENST00000706766.1:n.967_968del
ENST00000366955.8:c.8868_8869del MANE Select ENSP00000355922.3:p.Ser2957GlnfsTer18
ENST00000366955.7:c.8868_8869del ENSP00000355922.3:p.Ser2957GlnfsTer18
ENST00000469862.1:n.639_640del
NM_016343.3:c.8868_8869del NP_057427.3:p.Ser2957GlnfsTer18
XM_011509082.1:c.8691_8692del XP_011507384.1:p.Ser2898GlnfsTer18
XM_011509083.1:c.7803_7804del XP_011507385.1:p.Ser2602GlnfsTer18
XM_011509082.3:c.8691_8692del XP_011507384.1:p.Ser2898GlnfsTer18
XM_017000086.2:c.8868_8869del XP_016855575.1:p.Ser2957GlnfsTer18
NM_016343.4:c.8868_8869del MANE Select NP_057427.3:p.Ser2957GlnfsTer18