Canonical Allele Identifier: CA345802387

Gene: KLF11

Linked Data

• dbSNP Id: rs1225913271
• gnomAD v2: 2-10188227-G-A
• gnomAD v3: 2-10048100-G-A
• gnomAD v4: 2-10048100-G-A
• MyVariant Identifiers: chr2:g.10188227G>A (hg19) ; chr2:g.10048100G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048100G>A , CM000664.2:g.10048100G>A	GRCh38
NC_000002.11:g.10188227G>A , CM000664.1:g.10188227G>A	GRCh37
NC_000002.10:g.10105678G>A	NCBI36
NG_017199.1:g.9546G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.763G>A MANE Select	ENSP00000307023.1:p.Ala255Thr
ENST00000305883.5:c.763G>A	ENSP00000307023.1:p.Ala255Thr
ENST00000535335.1:c.712G>A	ENSP00000442722.1:p.Ala238Thr
ENST00000540845.5:c.712G>A	ENSP00000444690.1:p.Ala238Thr
NM_001177716.1:c.712G>A	NP_001171187.1:p.Ala238Thr
NM_001177718.1:c.712G>A	NP_001171189.1:p.Ala238Thr
NM_003597.4:c.763G>A	NP_003588.1:p.Ala255Thr
XM_005246179.3:c.712G>A	XP_005246236.1:p.Ala238Thr
NM_003597.5:c.763G>A MANE Select	NP_003588.1:p.Ala255Thr
NM_001177716.2:c.712G>A	NP_001171187.1:p.Ala238Thr
NM_001177718.2:c.712G>A	NP_001171189.1:p.Ala238Thr