Canonical Allele Identifier: CA2488331442

Gene: KLF11

Linked Data

• dbSNP Id: rs1661282216

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048204_10048206del , CM000664.2:g.10048204_10048206del	GRCh38
NC_000002.11:g.10188331_10188333del , CM000664.1:g.10188331_10188333del	GRCh37
NC_000002.10:g.10105782_10105784del	NCBI36
NG_017199.1:g.9650_9652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.867_869del MANE Select	ENSP00000307023.1:p.Met289del
ENST00000305883.5:c.867_869del	ENSP00000307023.1:p.Met289del
ENST00000535335.1:c.816_818del	ENSP00000442722.1:p.Met272del
ENST00000540845.5:c.816_818del	ENSP00000444690.1:p.Met272del
NM_001177716.1:c.816_818del	NP_001171187.1:p.Met272del
NM_001177718.1:c.816_818del	NP_001171189.1:p.Met272del
NM_003597.4:c.867_869del	NP_003588.1:p.Met289del
XM_005246179.3:c.816_818del	XP_005246236.1:p.Met272del
NM_003597.5:c.867_869del MANE Select	NP_003588.1:p.Met289del
NM_001177716.2:c.816_818del	NP_001171187.1:p.Met272del
NM_001177718.2:c.816_818del	NP_001171189.1:p.Met272del