Canonical Allele Identifier: CA344857829
Gene: CENPF HGNC NCBI

Linked Data

dbSNP Id: rs1658669628

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657395A>G , CM000663.2:g.214657395A>G GRCh38
NC_000001.10:g.214830738A>G , CM000663.1:g.214830738A>G GRCh37
NC_000001.9:g.212897361A>G NCBI36
NG_046787.1:g.59217A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8771A>G ENSP00000516538.1:p.Glu2924Gly
ENST00000706766.1:n.1047A>G
ENST00000366955.8:c.8948A>G MANE Select ENSP00000355922.3:p.Glu2983Gly
ENST00000366955.7:c.8948A>G ENSP00000355922.3:p.Glu2983Gly
ENST00000469862.1:n.719A>G
NM_016343.3:c.8948A>G NP_057427.3:p.Glu2983Gly
XM_011509082.1:c.8771A>G XP_011507384.1:p.Glu2924Gly
XM_011509083.1:c.7883A>G XP_011507385.1:p.Glu2628Gly
XM_011509082.3:c.8771A>G XP_011507384.1:p.Glu2924Gly
XM_017000086.2:c.8948A>G XP_016855575.1:p.Glu2983Gly
NM_016343.4:c.8948A>G MANE Select NP_057427.3:p.Glu2983Gly