Canonical Allele Identifier: CA2608059597

Gene: KLF6

Linked Data

• gnomAD v4: 10-3781590-TGCAGTGGCGCCCACCAGCGGCCGCCCTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781592_3781620del , CM000672.2:g.3781592_3781620del	GRCh38
NC_000010.10:g.3823784_3823812del , CM000672.1:g.3823784_3823812del	GRCh37
NC_000010.9:g.3813784_3813812del	NCBI36
NG_012277.1:g.8663_8691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.676+22_676+50del MANE Select	ENSP00000419923.1:n.676+22_676+50del
ENST00000173785.4:n.257+176_257+204del
ENST00000469435.1:c.698_726del	ENSP00000419079.1:p.Arg233HisfsTer?
ENST00000497571.5:c.676+22_676+50del	ENSP00000419923.1:n.676+22_676+50del
ENST00000542957.1:c.676+22_676+50del	ENSP00000445301.1:n.676+22_676+50del
NM_001160124.1:c.550+148_550+176del	NP_001153596.1:n.550+148_550+176del
NM_001160125.1:c.676+22_676+50del	NP_001153597.1:n.676+22_676+50del
NM_001300.5:c.676+22_676+50del	NP_001291.3:n.676+22_676+50del
NR_027653.1:n.789+176_789+204del
NM_001300.6:c.676+22_676+50del MANE Select	NP_001291.3:n.676+22_676+50del
NM_001160124.2:c.550+148_550+176del	NP_001153596.1:n.550+148_550+176del
NR_027653.2:n.717+176_717+204del
NM_001160125.2:c.676+22_676+50del	NP_001153597.1:n.676+22_676+50del