Canonical Allele Identifier: CA2486377791

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657560G= , CM000663.2:g.214657560G=	GRCh38
NC_000001.10:g.214830903G= , CM000663.1:g.214830903G=	GRCh37
NC_000001.9:g.212897526G=	NCBI36
NG_046787.1:g.59382G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+151G=	ENSP00000516538.1:n.8785+151G=
ENST00000706766.1:n.1061+151G=
ENST00000366955.8:c.8962+151G= MANE Select	ENSP00000355922.3:n.8962+151G=
ENST00000366955.7:c.8962+151G=	ENSP00000355922.3:n.8962+151G=
NM_016343.3:c.8962+151G=	NP_057427.3:n.8962+151G=
XM_011509082.1:c.8785+151G=	XP_011507384.1:n.8785+151G=
XM_011509083.1:c.7897+151G=	XP_011507385.1:n.7897+151G=
XM_011509082.3:c.8785+151G=	XP_011507384.1:n.8785+151G=
XM_017000086.2:c.8962+151G=	XP_016855575.1:n.8962+151G=
NM_016343.4:c.8962+151G= MANE Select	NP_057427.3:n.8962+151G=