Canonical Allele Identifier: CA345803270

Gene: KLF11

Linked Data

• dbSNP Id: rs1661283116
• gnomAD v3: 2-10048222-A-C
• gnomAD v4: 2-10048222-A-C
• MyVariant Identifiers: chr2:g.10188349A>C (hg19) ; chr2:g.10048222A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048222A>C , CM000664.2:g.10048222A>C	GRCh38
NC_000002.11:g.10188349A>C , CM000664.1:g.10188349A>C	GRCh37
NC_000002.10:g.10105800A>C	NCBI36
NG_017199.1:g.9668A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.885A>C MANE Select	ENSP00000307023.1:p.Gln295His
ENST00000305883.5:c.885A>C	ENSP00000307023.1:p.Gln295His
ENST00000535335.1:c.834A>C	ENSP00000442722.1:p.Gln278His
ENST00000540845.5:c.834A>C	ENSP00000444690.1:p.Gln278His
NM_001177716.1:c.834A>C	NP_001171187.1:p.Gln278His
NM_001177718.1:c.834A>C	NP_001171189.1:p.Gln278His
NM_003597.4:c.885A>C	NP_003588.1:p.Gln295His
XM_005246179.3:c.834A>C	XP_005246236.1:p.Gln278His
NM_003597.5:c.885A>C MANE Select	NP_003588.1:p.Gln295His
NM_001177716.2:c.834A>C	NP_001171187.1:p.Gln278His
NM_001177718.2:c.834A>C	NP_001171189.1:p.Gln278His