Canonical Allele Identifier: CA913088738

Gene: KLF11

Linked Data

• dbSNP Id: rs1558348250
• gnomAD v4: 2-10048165-T-TTCTGTC
• MyVariant Identifiers: chr2:g.10188292_10188293insTCTGTC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048172_10048177dup , CM000664.2:g.10048172_10048177dup	GRCh38
NC_000002.11:g.10188299_10188304dup , CM000664.1:g.10188299_10188304dup	GRCh37
NC_000002.10:g.10105750_10105755dup	NCBI36
NG_017199.1:g.9618_9623dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.835_840dup MANE Select	ENSP00000307023.1:p.Val280_Pro281insSerVal
ENST00000305883.5:c.835_840dup	ENSP00000307023.1:p.Val280_Pro281insSerVal
ENST00000535335.1:c.784_789dup	ENSP00000442722.1:p.Val263_Pro264insSerVal
ENST00000540845.5:c.784_789dup	ENSP00000444690.1:p.Val263_Pro264insSerVal
NM_001177716.1:c.784_789dup	NP_001171187.1:p.Val263_Pro264insSerVal
NM_001177718.1:c.784_789dup	NP_001171189.1:p.Val263_Pro264insSerVal
NM_003597.4:c.835_840dup	NP_003588.1:p.Val280_Pro281insSerVal
XM_005246179.3:c.784_789dup	XP_005246236.1:p.Val263_Pro264insSerVal
NM_003597.5:c.835_840dup MANE Select	NP_003588.1:p.Val280_Pro281insSerVal
NM_001177716.2:c.784_789dup	NP_001171187.1:p.Val263_Pro264insSerVal
NM_001177718.2:c.784_789dup	NP_001171189.1:p.Val263_Pro264insSerVal