Canonical Allele Identifier: CA2486377597

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657078T= , CM000663.2:g.214657078T=	GRCh38
NC_000001.10:g.214830421T= , CM000663.1:g.214830421T=	GRCh37
NC_000001.9:g.212897044T=	NCBI36
NG_046787.1:g.58900T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8454T=	ENSP00000516538.1:p.Ala2818=
ENST00000706766.1:n.730T=
ENST00000366955.8:c.8631T= MANE Select	ENSP00000355922.3:p.Ala2877=
ENST00000366955.7:c.8631T=	ENSP00000355922.3:p.Ala2877=
ENST00000469862.1:n.402T=
NM_016343.3:c.8631T=	NP_057427.3:p.Ala2877=
XM_011509082.1:c.8454T=	XP_011507384.1:p.Ala2818=
XM_011509083.1:c.7566T=	XP_011507385.1:p.Ala2522=
XM_011509082.3:c.8454T=	XP_011507384.1:p.Ala2818=
XM_017000086.2:c.8631T=	XP_016855575.1:p.Ala2877=
NM_016343.4:c.8631T= MANE Select	NP_057427.3:p.Ala2877=