Canonical Allele Identifier: CA2657823108
Gene: KLF11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10048173_10048174del , CM000664.2:g.10048173_10048174del GRCh38
NC_000002.11:g.10188300_10188301del , CM000664.1:g.10188300_10188301del GRCh37
NC_000002.10:g.10105751_10105752del NCBI36
NG_017199.1:g.9619_9620del

Transcript Alleles

HGVS Amino-acid Change
ENST00000305883.6:c.836_837del MANE Select ENSP00000307023.1:p.Ser279CysfsTer18
ENST00000305883.5:c.836_837del ENSP00000307023.1:p.Ser279CysfsTer18
ENST00000535335.1:c.785_786del ENSP00000442722.1:p.Ser262CysfsTer18
ENST00000540845.5:c.785_786del ENSP00000444690.1:p.Ser262CysfsTer18
NM_001177716.1:c.785_786del NP_001171187.1:p.Ser262CysfsTer18
NM_001177718.1:c.785_786del NP_001171189.1:p.Ser262CysfsTer18
NM_003597.4:c.836_837del NP_003588.1:p.Ser279CysfsTer18
XM_005246179.3:c.785_786del XP_005246236.1:p.Ser262CysfsTer18
NM_003597.5:c.836_837del MANE Select NP_003588.1:p.Ser279CysfsTer18
NM_001177716.2:c.785_786del NP_001171187.1:p.Ser262CysfsTer18
NM_001177718.2:c.785_786del NP_001171189.1:p.Ser262CysfsTer18