Canonical Allele Identifier: CA2657823102

Gene: KLF11

Linked Data

• gnomAD v4: 2-10048068-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048069_10048070del , CM000664.2:g.10048069_10048070del	GRCh38
NC_000002.11:g.10188196_10188197del , CM000664.1:g.10188196_10188197del	GRCh37
NC_000002.10:g.10105647_10105648del	NCBI36
NG_017199.1:g.9515_9516del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.732_733del MANE Select	ENSP00000307023.1:p.Asp245GlnfsTer20
ENST00000305883.5:c.732_733del	ENSP00000307023.1:p.Asp245GlnfsTer20
ENST00000535335.1:c.681_682del	ENSP00000442722.1:p.Asp228GlnfsTer20
ENST00000540845.5:c.681_682del	ENSP00000444690.1:p.Asp228GlnfsTer20
NM_001177716.1:c.681_682del	NP_001171187.1:p.Asp228GlnfsTer20
NM_001177718.1:c.681_682del	NP_001171189.1:p.Asp228GlnfsTer20
NM_003597.4:c.732_733del	NP_003588.1:p.Asp245GlnfsTer20
XM_005246179.3:c.681_682del	XP_005246236.1:p.Asp228GlnfsTer20
NM_003597.5:c.732_733del MANE Select	NP_003588.1:p.Asp245GlnfsTer20
NM_001177716.2:c.681_682del	NP_001171187.1:p.Asp228GlnfsTer20
NM_001177718.2:c.681_682del	NP_001171189.1:p.Asp228GlnfsTer20