Canonical Allele Identifier: CA2747695877

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622252_214622253insACACCCCAAACACACC , CM000663.2:g.214622252_214622253insACACCCCAAACACACC	GRCh38
NC_000001.10:g.214795595_214795596insACACCCCAAACACACC , CM000663.1:g.214795595_214795596insACACCCCAAACACACC	GRCh37
NC_000001.9:g.212862218_212862219insACACCCCAAACACACC	NCBI36
NG_046787.1:g.24074_24075insACACCCCAAACACACC

Transcript Alleles

HGVS	Amino-acid change
ENST00000706764.1:n.1217_1218insACACCCCAAACACACC
ENST00000706765.1:c.1039_1040insACACCCCAAACACACC	ENSP00000516538.1:p.Thr347AsnfsTer?
ENST00000366955.8:c.1039_1040insACACCCCAAACACACC MANE Select	ENSP00000355922.3:p.Thr347AsnfsTer?
ENST00000366955.7:c.1039_1040insACACCCCAAACACACC	ENSP00000355922.3:p.Thr347AsnfsTer?
NM_016343.3:c.1039_1040insACACCCCAAACACACC	NP_057427.3:p.Thr347AsnfsTer?
XM_011509082.1:c.1039_1040insACACCCCAAACACACC	XP_011507384.1:p.Thr347AsnfsTer?
XM_011509082.3:c.1039_1040insACACCCCAAACACACC	XP_011507384.1:p.Thr347AsnfsTer?
XM_017000086.2:c.1039_1040insACACCCCAAACACACC	XP_016855575.1:p.Thr347AsnfsTer?
NM_016343.4:c.1039_1040insACACCCCAAACACACC MANE Select	NP_057427.3:p.Thr347AsnfsTer?