Canonical Allele Identifier: CA468166732
Gene: KLF6 HGNC NCBI

Linked Data

gnomAD v4: 10-3782014-G-T
MyVariant Identifiers: chr10:g.3824206G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3782014G>T , CM000672.2:g.3782014G>T GRCh38
NC_000010.10:g.3824206G>T , CM000672.1:g.3824206G>T GRCh37
NC_000010.9:g.3814206G>T NCBI36
NG_012277.1:g.8268C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.303C>A MANE Select ENSP00000419923.1:p.Thr101=
ENST00000173785.4:n.38C>A
ENST00000380946.3:n.538C>A
ENST00000469435.1:c.303C>A ENSP00000419079.1:p.Thr101=
ENST00000497571.5:c.303C>A ENSP00000419923.1:p.Thr101=
ENST00000542957.1:c.303C>A ENSP00000445301.1:p.Thr101=
NM_001160124.1:c.303C>A NP_001153596.1:p.Thr101=
NM_001160125.1:c.303C>A NP_001153597.1:p.Thr101=
NM_001300.5:c.303C>A NP_001291.3:p.Thr101=
NR_027653.1:n.570C>A
NM_001300.6:c.303C>A MANE Select NP_001291.3:p.Thr101=
NM_001160124.2:c.303C>A NP_001153596.1:p.Thr101=
NR_027653.2:n.498C>A
NM_001160125.2:c.303C>A NP_001153597.1:p.Thr101=