Canonical Allele Identifier: CA2571585086
Gene: KLF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781659_3781660insGATAAACTCGCGGGTGCCATTACGGGCGGACTCATCGGCATTACGGCAATCTGGGTCGGCATGACGAGCGGCGCAACGGCGGCGACGATTACGCCGGAGAACCTTTTCAACTTCAAACTCGTGATGTT , CM000672.2:g.3781659_3781660insGATAAACTCGCGGGTGCCATTACGGGCGGACTCATCGGCATTACGGCAATCTGGGTCGGCATGACGAGCGGCGCAACGGCGGCGACGATTACGCCGGAGAACCTTTTCAACTTCAAACTCGTGATGTT GRCh38
NC_000010.10:g.3823851_3823852insGATAAACTCGCGGGTGCCATTACGGGCGGACTCATCGGCATTACGGCAATCTGGGTCGGCATGACGAGCGGCGCAACGGCGGCGACGATTACGCCGGAGAACCTTTTCAACTTCAAACTCGTGATGTT , CM000672.1:g.3823851_3823852insGATAAACTCGCGGGTGCCATTACGGGCGGACTCATCGGCATTACGGCAATCTGGGTCGGCATGACGAGCGGCGCAACGGCGGCGACGATTACGCCGGAGAACCTTTTCAACTTCAAACTCGTGATGTT GRCh37
NC_000010.9:g.3813851_3813852insGATAAACTCGCGGGTGCCATTACGGGCGGACTCATCGGCATTACGGCAATCTGGGTCGGCATGACGAGCGGCGCAACGGCGGCGACGATTACGCCGGAGAACCTTTTCAACTTCAAACTCGTGATGTT NCBI36
NG_012277.1:g.8622_8623insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC

Transcript Alleles

HGVS Amino-acid change
ENST00000497571.6:c.657_658insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC MANE Select ENSP00000419923.1:p.His220AsnfsTer71
ENST00000173785.4:n.257+135_257+136insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC
ENST00000469435.1:c.657_658insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC ENSP00000419079.1:p.His220AsnfsTer?
ENST00000497571.5:c.657_658insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC ENSP00000419923.1:p.His220AsnfsTer71
ENST00000542957.1:c.657_658insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC ENSP00000445301.1:p.His220AsnfsTer55
NM_001160124.1:c.550+107_550+108insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC NP_001153596.1:n.550+107_550+108insAACATCACGAGTTTGAAGTTGAAAAG...
NM_001160125.1:c.657_658insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC NP_001153597.1:p.His220AsnfsTer55
NM_001300.5:c.657_658insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC NP_001291.3:p.His220AsnfsTer71
NR_027653.1:n.789+135_789+136insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC
NM_001300.6:c.657_658insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC MANE Select NP_001291.3:p.His220AsnfsTer71
NM_001160124.2:c.550+107_550+108insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC NP_001153596.1:n.550+107_550+108insAACATCACGAGTTTGAAGTTGAAAAG...
NR_027653.2:n.717+135_717+136insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC
NM_001160125.2:c.657_658insAACATCACGAGTTTGAAGTTGAAAAGGTTCTCCGGCGTAATCGTCGCCGCCGTTGCGCCGCTCGTCATGCCGACCCAGATTGCCGTAATGCCGATGAGTCCGCCCGTAATGGCACCCGCGAGTTTATC NP_001153597.1:p.His220AsnfsTer55