Canonical Allele Identifier: CA2650488304

Gene: CENPF

Linked Data

• gnomAD v4: 1-214657474-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657479del , CM000663.2:g.214657479del	GRCh38
NC_000001.10:g.214830822del , CM000663.1:g.214830822del	GRCh37
NC_000001.9:g.212897445del	NCBI36
NG_046787.1:g.59301del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+70del	ENSP00000516538.1:n.8785+70del
ENST00000706766.1:n.1061+70del
ENST00000366955.8:c.8962+70del MANE Select	ENSP00000355922.3:n.8962+70del
ENST00000366955.7:c.8962+70del	ENSP00000355922.3:n.8962+70del
NM_016343.3:c.8962+70del	NP_057427.3:n.8962+70del
XM_011509082.1:c.8785+70del	XP_011507384.1:n.8785+70del
XM_011509083.1:c.7897+70del	XP_011507385.1:n.7897+70del
XM_011509082.3:c.8785+70del	XP_011507384.1:n.8785+70del
XM_017000086.2:c.8962+70del	XP_016855575.1:n.8962+70del
NM_016343.4:c.8962+70del MANE Select	NP_057427.3:n.8962+70del