Canonical Allele Identifier: CA2650488221

Gene: CENPF

Linked Data

• gnomAD v4: 1-214657118-CAGCAATCTAAACAAGATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657119_214657136del , CM000663.2:g.214657119_214657136del	GRCh38
NC_000001.10:g.214830462_214830479del , CM000663.1:g.214830462_214830479del	GRCh37
NC_000001.9:g.212897085_212897102del	NCBI36
NG_046787.1:g.58941_58958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8495_8512del	ENSP00000516538.1:p.Gln2832_Ser2838delinsPro
ENST00000706766.1:n.771_788del
ENST00000366955.8:c.8672_8689del MANE Select	ENSP00000355922.3:p.Gln2891_Ser2897delinsPro
ENST00000366955.7:c.8672_8689del	ENSP00000355922.3:p.Gln2891_Ser2897delinsPro
ENST00000469862.1:n.443_460del
NM_016343.3:c.8672_8689del	NP_057427.3:p.Gln2891_Ser2897delinsPro
XM_011509082.1:c.8495_8512del	XP_011507384.1:p.Gln2832_Ser2838delinsPro
XM_011509083.1:c.7607_7624del	XP_011507385.1:p.Gln2536_Ser2542delinsPro
XM_011509082.3:c.8495_8512del	XP_011507384.1:p.Gln2832_Ser2838delinsPro
XM_017000086.2:c.8672_8689del	XP_016855575.1:p.Gln2891_Ser2897delinsPro
NM_016343.4:c.8672_8689del MANE Select	NP_057427.3:p.Gln2891_Ser2897delinsPro