Canonical Allele Identifier: CA2488331371

Gene: KLF11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048066_10048070delinsCACTG , CM000664.2:g.10048066_10048070delinsCACTG	GRCh38
NC_000002.11:g.10188193_10188197delinsCACTG , CM000664.1:g.10188193_10188197delinsCACTG	GRCh37
NC_000002.10:g.10105644_10105648delinsCACTG	NCBI36
NG_017199.1:g.9512_9516delinsCACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.729_733delinsCACTG MANE Select	ENSP00000307023.1:p.Leu243=
ENST00000305883.5:c.729_733delinsCACTG	ENSP00000307023.1:p.Leu243=
ENST00000535335.1:c.678_682delinsCACTG	ENSP00000442722.1:p.Leu226=
ENST00000540845.5:c.678_682delinsCACTG	ENSP00000444690.1:p.Leu226=
NM_001177716.1:c.678_682delinsCACTG	NP_001171187.1:p.Leu226=
NM_001177718.1:c.678_682delinsCACTG	NP_001171189.1:p.Leu226=
NM_003597.4:c.729_733delinsCACTG	NP_003588.1:p.Leu243=
XM_005246179.3:c.678_682delinsCACTG	XP_005246236.1:p.Leu226=
NM_003597.5:c.729_733delinsCACTG MANE Select	NP_003588.1:p.Leu243=
NM_001177716.2:c.678_682delinsCACTG	NP_001171187.1:p.Leu226=
NM_001177718.2:c.678_682delinsCACTG	NP_001171189.1:p.Leu226=