Canonical Allele Identifier: CA345803197

Gene: KLF11

Linked Data

• dbSNP Id: rs1661282272
• gnomAD v3: 2-10048202-A-G
• gnomAD v4: 2-10048202-A-G
• MyVariant Identifiers: chr2:g.10188329A>G (hg19) ; chr2:g.10048202A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048202A>G , CM000664.2:g.10048202A>G	GRCh38
NC_000002.11:g.10188329A>G , CM000664.1:g.10188329A>G	GRCh37
NC_000002.10:g.10105780A>G	NCBI36
NG_017199.1:g.9648A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.865A>G MANE Select	ENSP00000307023.1:p.Met289Val
ENST00000305883.5:c.865A>G	ENSP00000307023.1:p.Met289Val
ENST00000535335.1:c.814A>G	ENSP00000442722.1:p.Met272Val
ENST00000540845.5:c.814A>G	ENSP00000444690.1:p.Met272Val
NM_001177716.1:c.814A>G	NP_001171187.1:p.Met272Val
NM_001177718.1:c.814A>G	NP_001171189.1:p.Met272Val
NM_003597.4:c.865A>G	NP_003588.1:p.Met289Val
XM_005246179.3:c.814A>G	XP_005246236.1:p.Met272Val
NM_003597.5:c.865A>G MANE Select	NP_003588.1:p.Met289Val
NM_001177716.2:c.814A>G	NP_001171187.1:p.Met272Val
NM_001177718.2:c.814A>G	NP_001171189.1:p.Met272Val