Canonical Allele Identifier: CA5388761
Gene: KLF6 HGNC NCBI

Linked Data

dbSNP Id: rs754239177
gnomAD v2: 10-3823976-C-T
gnomAD v3: 10-3781784-C-T
gnomAD v4: 10-3781784-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781784C>T , CM000672.2:g.3781784C>T GRCh38
NC_000010.10:g.3823976C>T , CM000672.1:g.3823976C>T GRCh37
NC_000010.9:g.3813976C>T NCBI36
NG_012277.1:g.8498G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.533G>A MANE Select ENSP00000419923.1:p.Gly178Glu
ENST00000173785.4:n.257+11G>A
ENST00000469435.1:c.533G>A ENSP00000419079.1:p.Gly178Glu
ENST00000497571.5:c.533G>A ENSP00000419923.1:p.Gly178Glu
ENST00000542957.1:c.533G>A ENSP00000445301.1:p.Gly178Glu
NM_001160124.1:c.533G>A NP_001153596.1:p.Gly178Glu
NM_001160125.1:c.533G>A NP_001153597.1:p.Gly178Glu
NM_001300.5:c.533G>A NP_001291.3:p.Gly178Glu
NR_027653.1:n.789+11G>A
NM_001300.6:c.533G>A MANE Select NP_001291.3:p.Gly178Glu
NM_001160124.2:c.533G>A NP_001153596.1:p.Gly178Glu
NR_027653.2:n.717+11G>A
NM_001160125.2:c.533G>A NP_001153597.1:p.Gly178Glu