Canonical Allele Identifier: CA2486377607

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657089T= , CM000663.2:g.214657089T=	GRCh38
NC_000001.10:g.214830432T= , CM000663.1:g.214830432T=	GRCh37
NC_000001.9:g.212897055T=	NCBI36
NG_046787.1:g.58911T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000706765.1:c.8465T=	ENSP00000516538.1:p.Leu2822=
ENST00000706766.1:n.741T=
ENST00000366955.8:c.8642T= MANE Select	ENSP00000355922.3:p.Leu2881=
ENST00000366955.7:c.8642T=	ENSP00000355922.3:p.Leu2881=
ENST00000469862.1:n.413T=
NM_016343.3:c.8642T=	NP_057427.3:p.Leu2881=
XM_011509082.1:c.8465T=	XP_011507384.1:p.Leu2822=
XM_011509083.1:c.7577T=	XP_011507385.1:p.Leu2526=
XM_011509082.3:c.8465T=	XP_011507384.1:p.Leu2822=
XM_017000086.2:c.8642T=	XP_016855575.1:p.Leu2881=
NM_016343.4:c.8642T= MANE Select	NP_057427.3:p.Leu2881=