Canonical Allele Identifier: CA153420

Gene: KLF11

Linked Data

• ClinVar Variation Id: 129430
• ClinVar RCV Id: RCV000117437 ; RCV000881038 ; RCV000664078
• dbSNP Id: rs145933214
• ExAC: 2:10187874 A / G
• gnomAD v2: 2-10187874-A-G
• gnomAD v3: 2-10047747-A-G
• gnomAD v4: 2-10047747-A-G
• MyVariant Identifiers: chr2:g.10187874A>G (hg19) ; chr2:g.10047747A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10047747A>G , CM000664.2:g.10047747A>G	GRCh38
NC_000002.11:g.10187874A>G , CM000664.1:g.10187874A>G	GRCh37
NC_000002.10:g.10105325A>G	NCBI36
NG_017199.1:g.9193A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.410A>G MANE Select	ENSP00000307023.1:p.Asp137Gly
ENST00000305883.5:c.410A>G	ENSP00000307023.1:p.Asp137Gly
ENST00000401510.5:c.359A>G	ENSP00000386058.1:p.Asp120Gly
ENST00000440320.5:c.359A>G	ENSP00000388263.1:p.Asp120Gly
ENST00000448523.5:c.359A>G	ENSP00000387866.1:p.Asp120Gly
ENST00000535335.1:c.359A>G	ENSP00000442722.1:p.Asp120Gly
ENST00000540845.5:c.359A>G	ENSP00000444690.1:p.Asp120Gly
NM_001177716.1:c.359A>G	NP_001171187.1:p.Asp120Gly
NM_001177718.1:c.359A>G	NP_001171189.1:p.Asp120Gly
NM_003597.4:c.410A>G	NP_003588.1:p.Asp137Gly
XM_005246179.3:c.359A>G	XP_005246236.1:p.Asp120Gly
NM_003597.5:c.410A>G MANE Select	NP_003588.1:p.Asp137Gly
NM_001177716.2:c.359A>G	NP_001171187.1:p.Asp120Gly
NM_001177718.2:c.359A>G	NP_001171189.1:p.Asp120Gly