Canonical Allele Identifier: CA1391509

Gene: CENPF

Linked Data

• dbSNP Id: rs745632367
• ExAC: 1:214830641 G / A
• gnomAD v2: 1-214830641-G-A
• MyVariant Identifiers: chr1:g.214830641G>A (hg19) ; chr1:g.214657298G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657298G>A , CM000663.2:g.214657298G>A	GRCh38
NC_000001.10:g.214830641G>A , CM000663.1:g.214830641G>A	GRCh37
NC_000001.9:g.212897264G>A	NCBI36
NG_046787.1:g.59120G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8674G>A	ENSP00000516538.1:p.Glu2892Lys
ENST00000706766.1:n.950G>A
ENST00000366955.8:c.8851G>A MANE Select	ENSP00000355922.3:p.Glu2951Lys
ENST00000366955.7:c.8851G>A	ENSP00000355922.3:p.Glu2951Lys
ENST00000469862.1:n.622G>A
NM_016343.3:c.8851G>A	NP_057427.3:p.Glu2951Lys
XM_011509082.1:c.8674G>A	XP_011507384.1:p.Glu2892Lys
XM_011509083.1:c.7786G>A	XP_011507385.1:p.Glu2596Lys
XM_011509082.3:c.8674G>A	XP_011507384.1:p.Glu2892Lys
XM_017000086.2:c.8851G>A	XP_016855575.1:p.Glu2951Lys
NM_016343.4:c.8851G>A MANE Select	NP_057427.3:p.Glu2951Lys