Canonical Allele Identifier: CA1390473
Gene: CENPF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214642149A>G , CM000663.2:g.214642149A>G GRCh38
NC_000001.10:g.214815492A>G , CM000663.1:g.214815492A>G GRCh37
NC_000001.9:g.212882115A>G NCBI36
NG_046787.1:g.43971A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.3811A>G ENSP00000516538.1:p.Lys1271Glu
ENST00000366955.8:c.3811A>G MANE Select ENSP00000355922.3:p.Lys1271Glu
ENST00000366955.7:c.3811A>G ENSP00000355922.3:p.Lys1271Glu
NM_016343.3:c.3811A>G NP_057427.3:p.Lys1271Glu
XM_011509082.1:c.3811A>G XP_011507384.1:p.Lys1271Glu
XM_011509083.1:c.2746A>G XP_011507385.1:p.Lys916Glu
XM_011509082.3:c.3811A>G XP_011507384.1:p.Lys1271Glu
XM_017000086.2:c.3811A>G XP_016855575.1:p.Lys1271Glu
NM_016343.4:c.3811A>G MANE Select NP_057427.3:p.Lys1271Glu