Canonical Allele Identifier: CA1027452494

Gene: KLF11

Linked Data

• dbSNP Id: rs1661281384
• gnomAD v3: 2-10048181-GCTC-G
• gnomAD v4: 2-10048181-GCTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048183_10048185del , CM000664.2:g.10048183_10048185del	GRCh38
NC_000002.11:g.10188310_10188312del , CM000664.1:g.10188310_10188312del	GRCh37
NC_000002.10:g.10105761_10105763del	NCBI36
NG_017199.1:g.9629_9631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.846_848del MANE Select	ENSP00000307023.1:p.Pro283del
ENST00000305883.5:c.846_848del	ENSP00000307023.1:p.Pro283del
ENST00000535335.1:c.795_797del	ENSP00000442722.1:p.Pro266del
ENST00000540845.5:c.795_797del	ENSP00000444690.1:p.Pro266del
NM_001177716.1:c.795_797del	NP_001171187.1:p.Pro266del
NM_001177718.1:c.795_797del	NP_001171189.1:p.Pro266del
NM_003597.4:c.846_848del	NP_003588.1:p.Pro283del
XM_005246179.3:c.795_797del	XP_005246236.1:p.Pro266del
NM_003597.5:c.846_848del MANE Select	NP_003588.1:p.Pro283del
NM_001177716.2:c.795_797del	NP_001171187.1:p.Pro266del
NM_001177718.2:c.795_797del	NP_001171189.1:p.Pro266del