Canonical Allele Identifier: CA2657823117

Gene: KLF11

Linked Data

• gnomAD v4: 2-10048274-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048274_10048275insG , CM000664.2:g.10048274_10048275insG	GRCh38
NC_000002.11:g.10188401_10188402insG , CM000664.1:g.10188401_10188402insG	GRCh37
NC_000002.10:g.10105852_10105853insG	NCBI36
NG_017199.1:g.9720_9721insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.937_938insG MANE Select	ENSP00000307023.1:p.Thr313SerfsTer?
ENST00000305883.5:c.937_938insG	ENSP00000307023.1:p.Thr313SerfsTer?
ENST00000535335.1:c.886_887insG	ENSP00000442722.1:p.Thr296SerfsTer?
ENST00000540845.5:c.886_887insG	ENSP00000444690.1:p.Thr296SerfsTer?
NM_001177716.1:c.886_887insG	NP_001171187.1:p.Thr296SerfsTer?
NM_001177718.1:c.886_887insG	NP_001171189.1:p.Thr296SerfsTer?
NM_003597.4:c.937_938insG	NP_003588.1:p.Thr313SerfsTer?
XM_005246179.3:c.886_887insG	XP_005246236.1:p.Thr296SerfsTer?
NM_003597.5:c.937_938insG MANE Select	NP_003588.1:p.Thr313SerfsTer?
NM_001177716.2:c.886_887insG	NP_001171187.1:p.Thr296SerfsTer?
NM_001177718.2:c.886_887insG	NP_001171189.1:p.Thr296SerfsTer?