Canonical Allele Identifier: CA1139796882

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657274A= , CM000663.2:g.214657274A=	GRCh38
NC_000001.10:g.214830617A= , CM000663.1:g.214830617A=	GRCh37
NC_000001.9:g.212897240A=	NCBI36
NG_046787.1:g.59096A=

Transcript Alleles

HGVS	Amino-acid Change
NM_016343.4:c.8827A= MANE Select	NP_057427.3:p.Arg2943=
ENST00000366955.8:c.8827A= MANE Select	ENSP00000355922.3:p.Arg2943=
NM_016343.3:c.8827A=	NP_057427.3:p.Arg2943=
ENST00000366955.7:c.8827A=	ENSP00000355922.3:p.Arg2943=
ENST00000469862.1:n.598A=
ENST00000706765.1:c.8650A=	ENSP00000516538.1:p.Arg2884=
ENST00000706766.1:n.926A=
XM_011509082.1:c.8650A=	XP_011507384.1:p.Arg2884=
XM_011509082.3:c.8650A=	XP_011507384.1:p.Arg2884=
XM_011509083.1:c.7762A=	XP_011507385.1:p.Arg2588=
XM_017000086.2:c.8827A=	XP_016855575.1:p.Arg2943=