Canonical Allele Identifier: CA1142137027

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622146A= , CM000663.2:g.214622146A=	GRCh38
NC_000001.10:g.214795489A= , CM000663.1:g.214795489A=	GRCh37
NC_000001.9:g.212862112A=	NCBI36
NG_046787.1:g.23968A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000706764.1:n.1111A=
ENST00000706765.1:c.933A=	ENSP00000516538.1:p.Gln311=
ENST00000366955.8:c.933A= MANE Select	ENSP00000355922.3:p.Gln311=
ENST00000366955.7:c.933A=	ENSP00000355922.3:p.Gln311=
NM_016343.3:c.933A=	NP_057427.3:p.Gln311=
XM_011509082.1:c.933A=	XP_011507384.1:p.Gln311=
XM_011509082.3:c.933A=	XP_011507384.1:p.Gln311=
XM_017000086.2:c.933A=	XP_016855575.1:p.Gln311=
NM_016343.4:c.933A= MANE Select	NP_057427.3:p.Gln311=