Canonical Allele Identifier: CA1141202227

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657412A= , CM000663.2:g.214657412A=	GRCh38
NC_000001.10:g.214830755A= , CM000663.1:g.214830755A=	GRCh37
NC_000001.9:g.212897378A=	NCBI36
NG_046787.1:g.59234A=

Transcript Alleles

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