Canonical Allele Identifier: CA2488331474
Gene: KLF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10048264G= , CM000664.2:g.10048264G= GRCh38
NC_000002.11:g.10188391G= , CM000664.1:g.10188391G= GRCh37
NC_000002.10:g.10105842G= NCBI36
NG_017199.1:g.9710G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305883.6:c.927G= MANE Select ENSP00000307023.1:p.Leu309=
ENST00000305883.5:c.927G= ENSP00000307023.1:p.Leu309=
ENST00000535335.1:c.876G= ENSP00000442722.1:p.Leu292=
ENST00000540845.5:c.876G= ENSP00000444690.1:p.Leu292=
NM_001177716.1:c.876G= NP_001171187.1:p.Leu292=
NM_001177718.1:c.876G= NP_001171189.1:p.Leu292=
NM_003597.4:c.927G= NP_003588.1:p.Leu309=
XM_005246179.3:c.876G= XP_005246236.1:p.Leu292=
NM_003597.5:c.927G= MANE Select NP_003588.1:p.Leu309=
NM_001177716.2:c.876G= NP_001171187.1:p.Leu292=
NM_001177718.2:c.876G= NP_001171189.1:p.Leu292=