Canonical Allele Identifier: CA468166658
Gene: KLF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.3824170A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781978A>T , CM000672.2:g.3781978A>T GRCh38
NC_000010.10:g.3824170A>T , CM000672.1:g.3824170A>T GRCh37
NC_000010.9:g.3814170A>T NCBI36
NG_012277.1:g.8304T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000497571.6:c.339T>A MANE Select ENSP00000419923.1:p.Ser113=
ENST00000173785.4:n.74T>A
ENST00000380946.3:n.574T>A
ENST00000469435.1:c.339T>A ENSP00000419079.1:p.Ser113=
ENST00000497571.5:c.339T>A ENSP00000419923.1:p.Ser113=
ENST00000542957.1:c.339T>A ENSP00000445301.1:p.Ser113=
NM_001160124.1:c.339T>A NP_001153596.1:p.Ser113=
NM_001160125.1:c.339T>A NP_001153597.1:p.Ser113=
NM_001300.5:c.339T>A NP_001291.3:p.Ser113=
NR_027653.1:n.606T>A
NM_001300.6:c.339T>A MANE Select NP_001291.3:p.Ser113=
NM_001160124.2:c.339T>A NP_001153596.1:p.Ser113=
NR_027653.2:n.534T>A
NM_001160125.2:c.339T>A NP_001153597.1:p.Ser113=