Canonical Allele Identifier: CA2486377662

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657206G= , CM000663.2:g.214657206G=	GRCh38
NC_000001.10:g.214830549G= , CM000663.1:g.214830549G=	GRCh37
NC_000001.9:g.212897172G=	NCBI36
NG_046787.1:g.59028G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8582G=	ENSP00000516538.1:p.Arg2861=
ENST00000706766.1:n.858G=
ENST00000366955.8:c.8759G= MANE Select	ENSP00000355922.3:p.Arg2920=
ENST00000366955.7:c.8759G=	ENSP00000355922.3:p.Arg2920=
ENST00000469862.1:n.530G=
NM_016343.3:c.8759G=	NP_057427.3:p.Arg2920=
XM_011509082.1:c.8582G=	XP_011507384.1:p.Arg2861=
XM_011509083.1:c.7694G=	XP_011507385.1:p.Arg2565=
XM_011509082.3:c.8582G=	XP_011507384.1:p.Arg2861=
XM_017000086.2:c.8759G=	XP_016855575.1:p.Arg2920=
NM_016343.4:c.8759G= MANE Select	NP_057427.3:p.Arg2920=