Canonical Allele Identifier: CA2486377657

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657188C= , CM000663.2:g.214657188C=	GRCh38
NC_000001.10:g.214830531C= , CM000663.1:g.214830531C=	GRCh37
NC_000001.9:g.212897154C=	NCBI36
NG_046787.1:g.59010C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8564C=	ENSP00000516538.1:p.Pro2855=
ENST00000706766.1:n.840C=
ENST00000366955.8:c.8741C= MANE Select	ENSP00000355922.3:p.Pro2914=
ENST00000366955.7:c.8741C=	ENSP00000355922.3:p.Pro2914=
ENST00000469862.1:n.512C=
NM_016343.3:c.8741C=	NP_057427.3:p.Pro2914=
XM_011509082.1:c.8564C=	XP_011507384.1:p.Pro2855=
XM_011509083.1:c.7676C=	XP_011507385.1:p.Pro2559=
XM_011509082.3:c.8564C=	XP_011507384.1:p.Pro2855=
XM_017000086.2:c.8741C=	XP_016855575.1:p.Pro2914=
NM_016343.4:c.8741C= MANE Select	NP_057427.3:p.Pro2914=