Canonical Allele Identifier: CA1525672

Gene: KLF11

Linked Data

• ClinVar Variation Id: 1645173
• ClinVar RCV Id: RCV002143734 ; RCV002505814
• dbSNP Id: rs145193520
• ExAC: 2:10188514 G / A
• gnomAD v2: 2-10188514-G-A
• gnomAD v3: 2-10048387-G-A
• gnomAD v4: 2-10048387-G-A
• MyVariant Identifiers: chr2:g.10188514G>A (hg19) ; chr2:g.10048387G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048387G>A , CM000664.2:g.10048387G>A	GRCh38
NC_000002.11:g.10188514G>A , CM000664.1:g.10188514G>A	GRCh37
NC_000002.10:g.10105965G>A	NCBI36
NG_017199.1:g.9833G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000305883.6:c.1050G>A MANE Select	ENSP00000307023.1:p.Pro350=
ENST00000305883.5:c.1050G>A	ENSP00000307023.1:p.Pro350=
ENST00000535335.1:c.999G>A	ENSP00000442722.1:p.Pro333=
ENST00000540845.5:c.999G>A	ENSP00000444690.1:p.Pro333=
NM_001177716.1:c.999G>A	NP_001171187.1:p.Pro333=
NM_001177718.1:c.999G>A	NP_001171189.1:p.Pro333=
NM_003597.4:c.1050G>A	NP_003588.1:p.Pro350=
XM_005246179.3:c.999G>A	XP_005246236.1:p.Pro333=
NM_003597.5:c.1050G>A MANE Select	NP_003588.1:p.Pro350=
NM_001177716.2:c.999G>A	NP_001171187.1:p.Pro333=
NM_001177718.2:c.999G>A	NP_001171189.1:p.Pro333=