Canonical Allele Identifier: CA2486364229

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622196A= , CM000663.2:g.214622196A=	GRCh38
NC_000001.10:g.214795539A= , CM000663.1:g.214795539A=	GRCh37
NC_000001.9:g.212862162A=	NCBI36
NG_046787.1:g.24018A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706764.1:n.1161A=
ENST00000706765.1:c.983A=	ENSP00000516538.1:p.Glu328=
ENST00000366955.8:c.983A= MANE Select	ENSP00000355922.3:p.Glu328=
ENST00000366955.7:c.983A=	ENSP00000355922.3:p.Glu328=
NM_016343.3:c.983A=	NP_057427.3:p.Glu328=
XM_011509082.1:c.983A=	XP_011507384.1:p.Glu328=
XM_011509082.3:c.983A=	XP_011507384.1:p.Glu328=
XM_017000086.2:c.983A=	XP_016855575.1:p.Glu328=
NM_016343.4:c.983A= MANE Select	NP_057427.3:p.Glu328=