Canonical Allele Identifier: CA1139656555

Gene: CENPF

Linked Data

• ClinVar Variation Id: 872564
• ClinVar RCV Id: RCV001093110
• dbSNP Id: rs1657291771

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214614829T>A , CM000663.2:g.214614829T>A	GRCh38
NC_000001.10:g.214788172T>A , CM000663.1:g.214788172T>A	GRCh37
NC_000001.9:g.212854795T>A	NCBI36
NG_046787.1:g.16651T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706764.1:n.341-3T>A
ENST00000706765.1:c.163-3T>A	ENSP00000516538.1:n.163-3T>A
ENST00000366955.8:c.163-3T>A MANE Select	ENSP00000355922.3:n.163-3T>A
ENST00000366955.7:c.163-3T>A	ENSP00000355922.3:n.163-3T>A
ENST00000464322.5:n.331-3T>A
NM_016343.3:c.163-3T>A	NP_057427.3:n.163-3T>A
XM_011509082.1:c.163-3T>A	XP_011507384.1:n.163-3T>A
XM_011509082.3:c.163-3T>A	XP_011507384.1:n.163-3T>A
XM_017000086.2:c.163-3T>A	XP_016855575.1:n.163-3T>A
NM_016343.4:c.163-3T>A MANE Select	NP_057427.3:n.163-3T>A