Canonical Allele Identifier: CA468166771
Gene: KLF6 HGNC NCBI

Linked Data

dbSNP Id: rs1832532297
MyVariant Identifiers: chr10:g.3824074G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781882G>A , CM000672.2:g.3781882G>A GRCh38
NC_000010.10:g.3824074G>A , CM000672.1:g.3824074G>A GRCh37
NC_000010.9:g.3814074G>A NCBI36
NG_012277.1:g.8400C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000497571.6:c.435C>T MANE Select ENSP00000419923.1:p.Thr145=
ENST00000173785.4:n.170C>T
ENST00000380946.3:n.670C>T
ENST00000469435.1:c.435C>T ENSP00000419079.1:p.Thr145=
ENST00000497571.5:c.435C>T ENSP00000419923.1:p.Thr145=
ENST00000542957.1:c.435C>T ENSP00000445301.1:p.Thr145=
NM_001160124.1:c.435C>T NP_001153596.1:p.Thr145=
NM_001160125.1:c.435C>T NP_001153597.1:p.Thr145=
NM_001300.5:c.435C>T NP_001291.3:p.Thr145=
NR_027653.1:n.702C>T
NM_001300.6:c.435C>T MANE Select NP_001291.3:p.Thr145=
NM_001160124.2:c.435C>T NP_001153596.1:p.Thr145=
NR_027653.2:n.630C>T
NM_001160125.2:c.435C>T NP_001153597.1:p.Thr145=