Canonical Allele Identifier: CA2488331452

Gene: KLF11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048216T= , CM000664.2:g.10048216T=	GRCh38
NC_000002.11:g.10188343T= , CM000664.1:g.10188343T=	GRCh37
NC_000002.10:g.10105794T=	NCBI36
NG_017199.1:g.9662T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.879T= MANE Select	ENSP00000307023.1:p.Thr293=
ENST00000305883.5:c.879T=	ENSP00000307023.1:p.Thr293=
ENST00000535335.1:c.828T=	ENSP00000442722.1:p.Thr276=
ENST00000540845.5:c.828T=	ENSP00000444690.1:p.Thr276=
NM_001177716.1:c.828T=	NP_001171187.1:p.Thr276=
NM_001177718.1:c.828T=	NP_001171189.1:p.Thr276=
NM_003597.4:c.879T=	NP_003588.1:p.Thr293=
XM_005246179.3:c.828T=	XP_005246236.1:p.Thr276=
NM_003597.5:c.879T= MANE Select	NP_003588.1:p.Thr293=
NM_001177716.2:c.828T=	NP_001171187.1:p.Thr276=
NM_001177718.2:c.828T=	NP_001171189.1:p.Thr276=