Canonical Allele Identifier: CA2486377815

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657636G= , CM000663.2:g.214657636G=	GRCh38
NC_000001.10:g.214830979G= , CM000663.1:g.214830979G=	GRCh37
NC_000001.9:g.212897602G=	NCBI36
NG_046787.1:g.59458G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+227G=	ENSP00000516538.1:n.8785+227G=
ENST00000706766.1:n.1061+227G=
ENST00000366955.8:c.8962+227G= MANE Select	ENSP00000355922.3:n.8962+227G=
ENST00000366955.7:c.8962+227G=	ENSP00000355922.3:n.8962+227G=
NM_016343.3:c.8962+227G=	NP_057427.3:n.8962+227G=
XM_011509082.1:c.8785+227G=	XP_011507384.1:n.8785+227G=
XM_011509083.1:c.7897+227G=	XP_011507385.1:n.7897+227G=
XM_011509082.3:c.8785+227G=	XP_011507384.1:n.8785+227G=
XM_017000086.2:c.8962+227G=	XP_016855575.1:n.8962+227G=
NM_016343.4:c.8962+227G= MANE Select	NP_057427.3:n.8962+227G=