Canonical Allele Identifier: CA2486377727

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657409G= , CM000663.2:g.214657409G=	GRCh38
NC_000001.10:g.214830752G= , CM000663.1:g.214830752G=	GRCh37
NC_000001.9:g.212897375G=	NCBI36
NG_046787.1:g.59231G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785G=	ENSP00000516538.1:p.Gly2929=
ENST00000706766.1:n.1061G=
ENST00000366955.8:c.8962G= MANE Select	ENSP00000355922.3:p.Gly2988=
ENST00000366955.7:c.8962G=	ENSP00000355922.3:p.Gly2988=
ENST00000469862.1:n.733G=
NM_016343.3:c.8962G=	NP_057427.3:p.Gly2988=
XM_011509082.1:c.8785G=	XP_011507384.1:p.Gly2929=
XM_011509083.1:c.7897G=	XP_011507385.1:p.Gly2633=
XM_011509082.3:c.8785G=	XP_011507384.1:p.Gly2929=
XM_017000086.2:c.8962G=	XP_016855575.1:p.Gly2988=
NM_016343.4:c.8962G= MANE Select	NP_057427.3:p.Gly2988=