Canonical Allele Identifier: CA2576674097
Gene: KLF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10048166del , CM000664.2:g.10048166del GRCh38
NC_000002.11:g.10188293del , CM000664.1:g.10188293del GRCh37
NC_000002.10:g.10105744del NCBI36
NG_017199.1:g.9612del

Transcript Alleles

HGVS Amino-acid Change
ENST00000305883.6:c.829del MANE Select ENSP00000307023.1:p.Ser277LeufsTer13
ENST00000305883.5:c.829del ENSP00000307023.1:p.Ser277LeufsTer13
ENST00000535335.1:c.778del ENSP00000442722.1:p.Ser260LeufsTer13
ENST00000540845.5:c.778del ENSP00000444690.1:p.Ser260LeufsTer13
NM_001177716.1:c.778del NP_001171187.1:p.Ser260LeufsTer13
NM_001177718.1:c.778del NP_001171189.1:p.Ser260LeufsTer13
NM_003597.4:c.829del NP_003588.1:p.Ser277LeufsTer13
XM_005246179.3:c.778del XP_005246236.1:p.Ser260LeufsTer13
NM_003597.5:c.829del MANE Select NP_003588.1:p.Ser277LeufsTer13
NM_001177716.2:c.778del NP_001171187.1:p.Ser260LeufsTer13
NM_001177718.2:c.778del NP_001171189.1:p.Ser260LeufsTer13