Canonical Allele Identifier: CA2488331441

Gene: KLF11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048200_10048203delinsAGAT , CM000664.2:g.10048200_10048203delinsAGAT	GRCh38
NC_000002.11:g.10188327_10188330delinsAGAT , CM000664.1:g.10188327_10188330delinsAGAT	GRCh37
NC_000002.10:g.10105778_10105781delinsAGAT	NCBI36
NG_017199.1:g.9646_9649delinsAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.863_866delinsAGAT MANE Select	ENSP00000307023.1:p.Gln288=
ENST00000305883.5:c.863_866delinsAGAT	ENSP00000307023.1:p.Gln288=
ENST00000535335.1:c.812_815delinsAGAT	ENSP00000442722.1:p.Gln271=
ENST00000540845.5:c.812_815delinsAGAT	ENSP00000444690.1:p.Gln271=
NM_001177716.1:c.812_815delinsAGAT	NP_001171187.1:p.Gln271=
NM_001177718.1:c.812_815delinsAGAT	NP_001171189.1:p.Gln271=
NM_003597.4:c.863_866delinsAGAT	NP_003588.1:p.Gln288=
XM_005246179.3:c.812_815delinsAGAT	XP_005246236.1:p.Gln271=
NM_003597.5:c.863_866delinsAGAT MANE Select	NP_003588.1:p.Gln288=
NM_001177716.2:c.812_815delinsAGAT	NP_001171187.1:p.Gln271=
NM_001177718.2:c.812_815delinsAGAT	NP_001171189.1:p.Gln271=