Canonical Allele Identifier: CA468166786
Gene: KLF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.3824095T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781903T>A , CM000672.2:g.3781903T>A GRCh38
NC_000010.10:g.3824095T>A , CM000672.1:g.3824095T>A GRCh37
NC_000010.9:g.3814095T>A NCBI36
NG_012277.1:g.8379A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.414A>T MANE Select ENSP00000419923.1:p.Gly138=
ENST00000173785.4:n.149A>T
ENST00000380946.3:n.649A>T
ENST00000469435.1:c.414A>T ENSP00000419079.1:p.Gly138=
ENST00000497571.5:c.414A>T ENSP00000419923.1:p.Gly138=
ENST00000542957.1:c.414A>T ENSP00000445301.1:p.Gly138=
NM_001160124.1:c.414A>T NP_001153596.1:p.Gly138=
NM_001160125.1:c.414A>T NP_001153597.1:p.Gly138=
NM_001300.5:c.414A>T NP_001291.3:p.Gly138=
NR_027653.1:n.681A>T
NM_001300.6:c.414A>T MANE Select NP_001291.3:p.Gly138=
NM_001160124.2:c.414A>T NP_001153596.1:p.Gly138=
NR_027653.2:n.609A>T
NM_001160125.2:c.414A>T NP_001153597.1:p.Gly138=