Canonical Allele Identifier: CA2657823119

Gene: KLF11

Linked Data

• gnomAD v4: 2-10048343-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048344_10048345del , CM000664.2:g.10048344_10048345del	GRCh38
NC_000002.11:g.10188471_10188472del , CM000664.1:g.10188471_10188472del	GRCh37
NC_000002.10:g.10105922_10105923del	NCBI36
NG_017199.1:g.9790_9791del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.1007_1008del MANE Select	ENSP00000307023.1:p.Gln336ArgfsTer?
ENST00000305883.5:c.1007_1008del	ENSP00000307023.1:p.Gln336ArgfsTer?
ENST00000535335.1:c.956_957del	ENSP00000442722.1:p.Gln319ArgfsTer?
ENST00000540845.5:c.956_957del	ENSP00000444690.1:p.Gln319ArgfsTer?
NM_001177716.1:c.956_957del	NP_001171187.1:p.Gln319ArgfsTer?
NM_001177718.1:c.956_957del	NP_001171189.1:p.Gln319ArgfsTer?
NM_003597.4:c.1007_1008del	NP_003588.1:p.Gln336ArgfsTer?
XM_005246179.3:c.956_957del	XP_005246236.1:p.Gln319ArgfsTer?
NM_003597.5:c.1007_1008del MANE Select	NP_003588.1:p.Gln336ArgfsTer?
NM_001177716.2:c.956_957del	NP_001171187.1:p.Gln319ArgfsTer?
NM_001177718.2:c.956_957del	NP_001171189.1:p.Gln319ArgfsTer?