Canonical Allele Identifier: CA345803720

Gene: KLF11

Linked Data

• dbSNP Id: rs929349988
• gnomAD v3: 2-10048391-G-C
• gnomAD v4: 2-10048391-G-C
• MyVariant Identifiers: chr2:g.10188518G>C (hg19) ; chr2:g.10048391G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048391G>C , CM000664.2:g.10048391G>C	GRCh38
NC_000002.11:g.10188518G>C , CM000664.1:g.10188518G>C	GRCh37
NC_000002.10:g.10105969G>C	NCBI36
NG_017199.1:g.9837G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.1054G>C MANE Select	ENSP00000307023.1:p.Ala352Pro
ENST00000305883.5:c.1054G>C	ENSP00000307023.1:p.Ala352Pro
ENST00000535335.1:c.1003G>C	ENSP00000442722.1:p.Ala335Pro
ENST00000540845.5:c.1003G>C	ENSP00000444690.1:p.Ala335Pro
NM_001177716.1:c.1003G>C	NP_001171187.1:p.Ala335Pro
NM_001177718.1:c.1003G>C	NP_001171189.1:p.Ala335Pro
NM_003597.4:c.1054G>C	NP_003588.1:p.Ala352Pro
XM_005246179.3:c.1003G>C	XP_005246236.1:p.Ala335Pro
NM_003597.5:c.1054G>C MANE Select	NP_003588.1:p.Ala352Pro
NM_001177716.2:c.1003G>C	NP_001171187.1:p.Ala335Pro
NM_001177718.2:c.1003G>C	NP_001171189.1:p.Ala335Pro