Canonical Allele Identifier: CA118893
Gene: KLF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 7572
ClinVar RCV Id: RCV000008008
dbSNP Id: rs121909142

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3782127A>G , CM000672.2:g.3782127A>G GRCh38
NC_000010.10:g.3824319A>G , CM000672.1:g.3824319A>G GRCh37
NC_000010.9:g.3814319A>G NCBI36
NG_012277.1:g.8155T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000497571.6:c.190T>C MANE Select ENSP00000419923.1:p.Trp64Arg
ENST00000380946.3:n.425T>C
ENST00000469435.1:c.190T>C ENSP00000419079.1:p.Trp64Arg
ENST00000497571.5:c.190T>C ENSP00000419923.1:p.Trp64Arg
ENST00000542957.1:c.190T>C ENSP00000445301.1:p.Trp64Arg
NM_001160124.1:c.190T>C NP_001153596.1:p.Trp64Arg
NM_001160125.1:c.190T>C NP_001153597.1:p.Trp64Arg
NM_001300.5:c.190T>C NP_001291.3:p.Trp64Arg
NR_027653.1:n.457T>C
NM_001300.6:c.190T>C MANE Select NP_001291.3:p.Trp64Arg
NM_001160124.2:c.190T>C NP_001153596.1:p.Trp64Arg
NR_027653.2:n.385T>C
NM_001160125.2:c.190T>C NP_001153597.1:p.Trp64Arg