Canonical Allele Identifier: CA2650488317

Gene: CENPF

Linked Data

• gnomAD v4: 1-214657493-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657493_214657494insT , CM000663.2:g.214657493_214657494insT	GRCh38
NC_000001.10:g.214830836_214830837insT , CM000663.1:g.214830836_214830837insT	GRCh37
NC_000001.9:g.212897459_212897460insT	NCBI36
NG_046787.1:g.59315_59316insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+84_8785+85insT	ENSP00000516538.1:n.8785+84_8785+85insT
ENST00000706766.1:n.1061+84_1061+85insT
ENST00000366955.8:c.8962+84_8962+85insT MANE Select	ENSP00000355922.3:n.8962+84_8962+85insT
ENST00000366955.7:c.8962+84_8962+85insT	ENSP00000355922.3:n.8962+84_8962+85insT
NM_016343.3:c.8962+84_8962+85insT	NP_057427.3:n.8962+84_8962+85insT
XM_011509082.1:c.8785+84_8785+85insT	XP_011507384.1:n.8785+84_8785+85insT
XM_011509083.1:c.7897+84_7897+85insT	XP_011507385.1:n.7897+84_7897+85insT
XM_011509082.3:c.8785+84_8785+85insT	XP_011507384.1:n.8785+84_8785+85insT
XM_017000086.2:c.8962+84_8962+85insT	XP_016855575.1:n.8962+84_8962+85insT
NM_016343.4:c.8962+84_8962+85insT MANE Select	NP_057427.3:n.8962+84_8962+85insT