Canonical Allele Identifier: CA2486377691

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657320A= , CM000663.2:g.214657320A=	GRCh38
NC_000001.10:g.214830663A= , CM000663.1:g.214830663A=	GRCh37
NC_000001.9:g.212897286A=	NCBI36
NG_046787.1:g.59142A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8696A=	ENSP00000516538.1:p.Lys2899=
ENST00000706766.1:n.972A=
ENST00000366955.8:c.8873A= MANE Select	ENSP00000355922.3:p.Lys2958=
ENST00000366955.7:c.8873A=	ENSP00000355922.3:p.Lys2958=
ENST00000469862.1:n.644A=
NM_016343.3:c.8873A=	NP_057427.3:p.Lys2958=
XM_011509082.1:c.8696A=	XP_011507384.1:p.Lys2899=
XM_011509083.1:c.7808A=	XP_011507385.1:p.Lys2603=
XM_011509082.3:c.8696A=	XP_011507384.1:p.Lys2899=
XM_017000086.2:c.8873A=	XP_016855575.1:p.Lys2958=
NM_016343.4:c.8873A= MANE Select	NP_057427.3:p.Lys2958=