Canonical Allele Identifier: CA2486377711

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657381A= , CM000663.2:g.214657381A=	GRCh38
NC_000001.10:g.214830724A= , CM000663.1:g.214830724A=	GRCh37
NC_000001.9:g.212897347A=	NCBI36
NG_046787.1:g.59203A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8757A=	ENSP00000516538.1:p.Pro2919=
ENST00000706766.1:n.1033A=
ENST00000366955.8:c.8934A= MANE Select	ENSP00000355922.3:p.Pro2978=
ENST00000366955.7:c.8934A=	ENSP00000355922.3:p.Pro2978=
ENST00000469862.1:n.705A=
NM_016343.3:c.8934A=	NP_057427.3:p.Pro2978=
XM_011509082.1:c.8757A=	XP_011507384.1:p.Pro2919=
XM_011509083.1:c.7869A=	XP_011507385.1:p.Pro2623=
XM_011509082.3:c.8757A=	XP_011507384.1:p.Pro2919=
XM_017000086.2:c.8934A=	XP_016855575.1:p.Pro2978=
NM_016343.4:c.8934A= MANE Select	NP_057427.3:p.Pro2978=