Canonical Allele Identifier: CA591841668

Gene: KLF6

Linked Data

• dbSNP Id: rs1208558882
• gnomAD v2: 10-3824281-TTCC-T
• gnomAD v4: 10-3782089-TTCC-T
• MyVariant Identifiers: chr10:g.3824282_3824284del (hg19) ; chr10:g.3782090_3782092del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3782094_3782096del , CM000672.2:g.3782094_3782096del	GRCh38
NC_000010.10:g.3824286_3824288del , CM000672.1:g.3824286_3824288del	GRCh37
NC_000010.9:g.3814286_3814288del	NCBI36
NG_012277.1:g.8190_8192del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.225_227del MANE Select	ENSP00000419923.1:p.Glu76del
ENST00000380946.3:n.460_462del
ENST00000469435.1:c.225_227del	ENSP00000419079.1:p.Glu76del
ENST00000497571.5:c.225_227del	ENSP00000419923.1:p.Glu76del
ENST00000542957.1:c.225_227del	ENSP00000445301.1:p.Glu76del
NM_001160124.1:c.225_227del	NP_001153596.1:p.Glu76del
NM_001160125.1:c.225_227del	NP_001153597.1:p.Glu76del
NM_001300.5:c.225_227del	NP_001291.3:p.Glu76del
NR_027653.1:n.492_494del
NM_001300.6:c.225_227del MANE Select	NP_001291.3:p.Glu76del
NM_001160124.2:c.225_227del	NP_001153596.1:p.Glu76del
NR_027653.2:n.420_422del
NM_001160125.2:c.225_227del	NP_001153597.1:p.Glu76del