Canonical Allele Identifier: CA344832910
Gene: CENPF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214622151A>C , CM000663.2:g.214622151A>C GRCh38
NC_000001.10:g.214795494A>C , CM000663.1:g.214795494A>C GRCh37
NC_000001.9:g.212862117A>C NCBI36
NG_046787.1:g.23973A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706764.1:n.1116A>C
ENST00000706765.1:c.938A>C ENSP00000516538.1:p.Asn313Thr
ENST00000366955.8:c.938A>C MANE Select ENSP00000355922.3:p.Asn313Thr
ENST00000366955.7:c.938A>C ENSP00000355922.3:p.Asn313Thr
NM_016343.3:c.938A>C NP_057427.3:p.Asn313Thr
XM_011509082.1:c.938A>C XP_011507384.1:p.Asn313Thr
XM_011509082.3:c.938A>C XP_011507384.1:p.Asn313Thr
XM_017000086.2:c.938A>C XP_016855575.1:p.Asn313Thr
NM_016343.4:c.938A>C MANE Select NP_057427.3:p.Asn313Thr