Canonical Allele Identifier: CA1148250855

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657298G= , CM000663.2:g.214657298G=	GRCh38
NC_000001.10:g.214830641G= , CM000663.1:g.214830641G=	GRCh37
NC_000001.9:g.212897264G=	NCBI36
NG_046787.1:g.59120G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8674G=	ENSP00000516538.1:p.Glu2892=
ENST00000706766.1:n.950G=
ENST00000366955.8:c.8851G= MANE Select	ENSP00000355922.3:p.Glu2951=
ENST00000366955.7:c.8851G=	ENSP00000355922.3:p.Glu2951=
ENST00000469862.1:n.622G=
NM_016343.3:c.8851G=	NP_057427.3:p.Glu2951=
XM_011509082.1:c.8674G=	XP_011507384.1:p.Glu2892=
XM_011509083.1:c.7786G=	XP_011507385.1:p.Glu2596=
XM_011509082.3:c.8674G=	XP_011507384.1:p.Glu2892=
XM_017000086.2:c.8851G=	XP_016855575.1:p.Glu2951=
NM_016343.4:c.8851G= MANE Select	NP_057427.3:p.Glu2951=