Canonical Allele Identifier: CA2488331522

Gene: KLF11

Linked Data

• dbSNP Id: rs1661295666

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048351_10048377del , CM000664.2:g.10048351_10048377del	GRCh38
NC_000002.11:g.10188478_10188504del , CM000664.1:g.10188478_10188504del	GRCh37
NC_000002.10:g.10105929_10105955del	NCBI36
NG_017199.1:g.9797_9823del

Transcript Alleles

HGVS	Amino-acid change
ENST00000305883.6:c.1014_1040del MANE Select	ENSP00000307023.1:p.Val339_Ala347del
ENST00000305883.5:c.1014_1040del	ENSP00000307023.1:p.Val339_Ala347del
ENST00000535335.1:c.963_989del	ENSP00000442722.1:p.Val322_Ala330del
ENST00000540845.5:c.963_989del	ENSP00000444690.1:p.Val322_Ala330del
NM_001177716.1:c.963_989del	NP_001171187.1:p.Val322_Ala330del
NM_001177718.1:c.963_989del	NP_001171189.1:p.Val322_Ala330del
NM_003597.4:c.1014_1040del	NP_003588.1:p.Val339_Ala347del
XM_005246179.3:c.963_989del	XP_005246236.1:p.Val322_Ala330del
NM_003597.5:c.1014_1040del MANE Select	NP_003588.1:p.Val339_Ala347del
NM_001177716.2:c.963_989del	NP_001171187.1:p.Val322_Ala330del
NM_001177718.2:c.963_989del	NP_001171189.1:p.Val322_Ala330del