Canonical Allele Identifier: CA344833230
Gene: CENPF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214622202T>A , CM000663.2:g.214622202T>A GRCh38
NC_000001.10:g.214795545T>A , CM000663.1:g.214795545T>A GRCh37
NC_000001.9:g.212862168T>A NCBI36
NG_046787.1:g.24024T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706764.1:n.1167T>A
ENST00000706765.1:c.989T>A ENSP00000516538.1:p.Ile330Asn
ENST00000366955.8:c.989T>A MANE Select ENSP00000355922.3:p.Ile330Asn
ENST00000366955.7:c.989T>A ENSP00000355922.3:p.Ile330Asn
NM_016343.3:c.989T>A NP_057427.3:p.Ile330Asn
XM_011509082.1:c.989T>A XP_011507384.1:p.Ile330Asn
XM_011509082.3:c.989T>A XP_011507384.1:p.Ile330Asn
XM_017000086.2:c.989T>A XP_016855575.1:p.Ile330Asn
NM_016343.4:c.989T>A MANE Select NP_057427.3:p.Ile330Asn