Canonical Allele Identifier: CA1139794922
Gene: CENPF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657565A= , CM000663.2:g.214657565A= GRCh38
NC_000001.10:g.214830908A= , CM000663.1:g.214830908A= GRCh37
NC_000001.9:g.212897531A= NCBI36
NG_046787.1:g.59387A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8785+156A= ENSP00000516538.1:n.8785+156A=
ENST00000706766.1:n.1061+156A=
ENST00000366955.8:c.8962+156A= MANE Select ENSP00000355922.3:n.8962+156A=
ENST00000366955.7:c.8962+156A= ENSP00000355922.3:n.8962+156A=
NM_016343.3:c.8962+156A= NP_057427.3:n.8962+156A=
XM_011509082.1:c.8785+156A= XP_011507384.1:n.8785+156A=
XM_011509083.1:c.7897+156A= XP_011507385.1:n.7897+156A=
XM_011509082.3:c.8785+156A= XP_011507384.1:n.8785+156A=
XM_017000086.2:c.8962+156A= XP_016855575.1:n.8962+156A=
NM_016343.4:c.8962+156A= MANE Select NP_057427.3:n.8962+156A=
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