Canonical Allele Identifier: CA1142396358

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657248G= , CM000663.2:g.214657248G=	GRCh38
NC_000001.10:g.214830591G= , CM000663.1:g.214830591G=	GRCh37
NC_000001.9:g.212897214G=	NCBI36
NG_046787.1:g.59070G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8624G=	ENSP00000516538.1:p.Arg2875=
ENST00000706766.1:n.900G=
ENST00000366955.8:c.8801G= MANE Select	ENSP00000355922.3:p.Arg2934=
ENST00000366955.7:c.8801G=	ENSP00000355922.3:p.Arg2934=
ENST00000469862.1:n.572G=
NM_016343.3:c.8801G=	NP_057427.3:p.Arg2934=
XM_011509082.1:c.8624G=	XP_011507384.1:p.Arg2875=
XM_011509083.1:c.7736G=	XP_011507385.1:p.Arg2579=
XM_011509082.3:c.8624G=	XP_011507384.1:p.Arg2875=
XM_017000086.2:c.8801G=	XP_016855575.1:p.Arg2934=
NM_016343.4:c.8801G= MANE Select	NP_057427.3:p.Arg2934=