Canonical Allele Identifier: CA2650488282

Gene: CENPF

Linked Data

• gnomAD v4: 1-214657202-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657205_214657206del , CM000663.2:g.214657205_214657206del	GRCh38
NC_000001.10:g.214830548_214830549del , CM000663.1:g.214830548_214830549del	GRCh37
NC_000001.9:g.212897171_212897172del	NCBI36
NG_046787.1:g.59027_59028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8581_8582del	ENSP00000516538.1:p.Arg2861ValfsTer7
ENST00000706766.1:n.857_858del
ENST00000366955.8:c.8758_8759del MANE Select	ENSP00000355922.3:p.Arg2920ValfsTer7
ENST00000366955.7:c.8758_8759del	ENSP00000355922.3:p.Arg2920ValfsTer7
ENST00000469862.1:n.529_530del
NM_016343.3:c.8758_8759del	NP_057427.3:p.Arg2920ValfsTer7
XM_011509082.1:c.8581_8582del	XP_011507384.1:p.Arg2861ValfsTer7
XM_011509083.1:c.7693_7694del	XP_011507385.1:p.Arg2565ValfsTer7
XM_011509082.3:c.8581_8582del	XP_011507384.1:p.Arg2861ValfsTer7
XM_017000086.2:c.8758_8759del	XP_016855575.1:p.Arg2920ValfsTer7
NM_016343.4:c.8758_8759del MANE Select	NP_057427.3:p.Arg2920ValfsTer7