Canonical Allele Identifier: CA2650488286

Gene: CENPF

Linked Data

• gnomAD v4: 1-214657414-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657414G>A , CM000663.2:g.214657414G>A	GRCh38
NC_000001.10:g.214830757G>A , CM000663.1:g.214830757G>A	GRCh37
NC_000001.9:g.212897380G>A	NCBI36
NG_046787.1:g.59236G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+5G>A	ENSP00000516538.1:n.8785+5G>A
ENST00000706766.1:n.1061+5G>A
ENST00000366955.8:c.8962+5G>A MANE Select	ENSP00000355922.3:n.8962+5G>A
ENST00000366955.7:c.8962+5G>A	ENSP00000355922.3:n.8962+5G>A
NM_016343.3:c.8962+5G>A	NP_057427.3:n.8962+5G>A
XM_011509082.1:c.8785+5G>A	XP_011507384.1:n.8785+5G>A
XM_011509083.1:c.7897+5G>A	XP_011507385.1:n.7897+5G>A
XM_011509082.3:c.8785+5G>A	XP_011507384.1:n.8785+5G>A
XM_017000086.2:c.8962+5G>A	XP_016855575.1:n.8962+5G>A
NM_016343.4:c.8962+5G>A MANE Select	NP_057427.3:n.8962+5G>A