Canonical Allele Identifier: CA2488331372
Gene: KLF11 HGNC NCBI

Linked Data

dbSNP Id: rs1661276258

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10048069_10048072del , CM000664.2:g.10048069_10048072del GRCh38
NC_000002.11:g.10188196_10188199del , CM000664.1:g.10188196_10188199del GRCh37
NC_000002.10:g.10105647_10105650del NCBI36
NG_017199.1:g.9515_9518del

Transcript Alleles

HGVS Amino-acid Change
ENST00000305883.6:c.732_735del MANE Select ENSP00000307023.1:p.Asp245LysfsTer?
ENST00000305883.5:c.732_735del ENSP00000307023.1:p.Asp245LysfsTer?
ENST00000535335.1:c.681_684del ENSP00000442722.1:p.Asp228LysfsTer?
ENST00000540845.5:c.681_684del ENSP00000444690.1:p.Asp228LysfsTer?
NM_001177716.1:c.681_684del NP_001171187.1:p.Asp228LysfsTer?
NM_001177718.1:c.681_684del NP_001171189.1:p.Asp228LysfsTer?
NM_003597.4:c.732_735del NP_003588.1:p.Asp245LysfsTer?
XM_005246179.3:c.681_684del XP_005246236.1:p.Asp228LysfsTer?
NM_003597.5:c.732_735del MANE Select NP_003588.1:p.Asp245LysfsTer?
NM_001177716.2:c.681_684del NP_001171187.1:p.Asp228LysfsTer?
NM_001177718.2:c.681_684del NP_001171189.1:p.Asp228LysfsTer?