Canonical Allele Identifier: CA1525636

Gene: KLF11

Linked Data

• dbSNP Id: rs752317241
• ExAC: 2:10188396 T / C
• gnomAD v2: 2-10188396-T-C
• gnomAD v3: 2-10048269-T-C
• gnomAD v4: 2-10048269-T-C
• MyVariant Identifiers: chr2:g.10188396T>C (hg19) ; chr2:g.10048269T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048269T>C , CM000664.2:g.10048269T>C	GRCh38
NC_000002.11:g.10188396T>C , CM000664.1:g.10188396T>C	GRCh37
NC_000002.10:g.10105847T>C	NCBI36
NG_017199.1:g.9715T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.932T>C MANE Select	ENSP00000307023.1:p.Val311Ala
ENST00000305883.5:c.932T>C	ENSP00000307023.1:p.Val311Ala
ENST00000535335.1:c.881T>C	ENSP00000442722.1:p.Val294Ala
ENST00000540845.5:c.881T>C	ENSP00000444690.1:p.Val294Ala
NM_001177716.1:c.881T>C	NP_001171187.1:p.Val294Ala
NM_001177718.1:c.881T>C	NP_001171189.1:p.Val294Ala
NM_003597.4:c.932T>C	NP_003588.1:p.Val311Ala
XM_005246179.3:c.881T>C	XP_005246236.1:p.Val294Ala
NM_003597.5:c.932T>C MANE Select	NP_003588.1:p.Val311Ala
NM_001177716.2:c.881T>C	NP_001171187.1:p.Val294Ala
NM_001177718.2:c.881T>C	NP_001171189.1:p.Val294Ala