Canonical Allele Identifier: CA2486377717
Gene: CENPF HGNC NCBI

Linked Data

dbSNP Id: rs1658669224

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214657386_214657387insTA , CM000663.2:g.214657386_214657387insTA GRCh38
NC_000001.10:g.214830729_214830730insTA , CM000663.1:g.214830729_214830730insTA GRCh37
NC_000001.9:g.212897352_212897353insTA NCBI36
NG_046787.1:g.59208_59209insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706765.1:c.8762_8763insTA ENSP00000516538.1:p.Leu2922AsnfsTer6
ENST00000706766.1:n.1038_1039insTA
ENST00000366955.8:c.8939_8940insTA MANE Select ENSP00000355922.3:p.Leu2981AsnfsTer6
ENST00000366955.7:c.8939_8940insTA ENSP00000355922.3:p.Leu2981AsnfsTer6
ENST00000469862.1:n.710_711insTA
NM_016343.3:c.8939_8940insTA NP_057427.3:p.Leu2981AsnfsTer6
XM_011509082.1:c.8762_8763insTA XP_011507384.1:p.Leu2922AsnfsTer6
XM_011509083.1:c.7874_7875insTA XP_011507385.1:p.Leu2626AsnfsTer6
XM_011509082.3:c.8762_8763insTA XP_011507384.1:p.Leu2922AsnfsTer6
XM_017000086.2:c.8939_8940insTA XP_016855575.1:p.Leu2981AsnfsTer6
NM_016343.4:c.8939_8940insTA MANE Select NP_057427.3:p.Leu2981AsnfsTer6