Canonical Allele Identifier: CA344834267
Gene: CENPF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214622241T>G , CM000663.2:g.214622241T>G GRCh38
NC_000001.10:g.214795584T>G , CM000663.1:g.214795584T>G GRCh37
NC_000001.9:g.212862207T>G NCBI36
NG_046787.1:g.24063T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706764.1:n.1206T>G
ENST00000706765.1:c.1028T>G ENSP00000516538.1:p.Leu343Arg
ENST00000366955.8:c.1028T>G MANE Select ENSP00000355922.3:p.Leu343Arg
ENST00000366955.7:c.1028T>G ENSP00000355922.3:p.Leu343Arg
NM_016343.3:c.1028T>G NP_057427.3:p.Leu343Arg
XM_011509082.1:c.1028T>G XP_011507384.1:p.Leu343Arg
XM_011509082.3:c.1028T>G XP_011507384.1:p.Leu343Arg
XM_017000086.2:c.1028T>G XP_016855575.1:p.Leu343Arg
NM_016343.4:c.1028T>G MANE Select NP_057427.3:p.Leu343Arg