Canonical Allele Identifier: CA2486377802
Gene: CENPF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657595T= , CM000663.2:g.214657595T= GRCh38
NC_000001.10:g.214830938T= , CM000663.1:g.214830938T= GRCh37
NC_000001.9:g.212897561T= NCBI36
NG_046787.1:g.59417T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8785+186T= ENSP00000516538.1:n.8785+186T=
ENST00000706766.1:n.1061+186T=
ENST00000366955.8:c.8962+186T= MANE Select ENSP00000355922.3:n.8962+186T=
ENST00000366955.7:c.8962+186T= ENSP00000355922.3:n.8962+186T=
NM_016343.3:c.8962+186T= NP_057427.3:n.8962+186T=
XM_011509082.1:c.8785+186T= XP_011507384.1:n.8785+186T=
XM_011509083.1:c.7897+186T= XP_011507385.1:n.7897+186T=
XM_011509082.3:c.8785+186T= XP_011507384.1:n.8785+186T=
XM_017000086.2:c.8962+186T= XP_016855575.1:n.8962+186T=
NM_016343.4:c.8962+186T= MANE Select NP_057427.3:n.8962+186T=
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