Canonical Allele Identifier: CA1012114952
Gene: CENPF HGNC NCBI

Linked Data

dbSNP Id: rs1658675476
gnomAD v3: 1-214657591-C-A
gnomAD v4: 1-214657591-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657591C>A , CM000663.2:g.214657591C>A GRCh38
NC_000001.10:g.214830934C>A , CM000663.1:g.214830934C>A GRCh37
NC_000001.9:g.212897557C>A NCBI36
NG_046787.1:g.59413C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8785+182C>A ENSP00000516538.1:n.8785+182C>A
ENST00000706766.1:n.1061+182C>A
ENST00000366955.8:c.8962+182C>A MANE Select ENSP00000355922.3:n.8962+182C>A
ENST00000366955.7:c.8962+182C>A ENSP00000355922.3:n.8962+182C>A
NM_016343.3:c.8962+182C>A NP_057427.3:n.8962+182C>A
XM_011509082.1:c.8785+182C>A XP_011507384.1:n.8785+182C>A
XM_011509083.1:c.7897+182C>A XP_011507385.1:n.7897+182C>A
XM_011509082.3:c.8785+182C>A XP_011507384.1:n.8785+182C>A
XM_017000086.2:c.8962+182C>A XP_016855575.1:n.8962+182C>A
NM_016343.4:c.8962+182C>A MANE Select NP_057427.3:n.8962+182C>A
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