Canonical Allele Identifier: CA468166705
Gene: KLF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.3824014C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781822C>G , CM000672.2:g.3781822C>G GRCh38
NC_000010.10:g.3824014C>G , CM000672.1:g.3824014C>G GRCh37
NC_000010.9:g.3814014C>G NCBI36
NG_012277.1:g.8460G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.495G>C MANE Select ENSP00000419923.1:p.Val165=
ENST00000173785.4:n.230G>C
ENST00000380946.3:n.730G>C
ENST00000469435.1:c.495G>C ENSP00000419079.1:p.Val165=
ENST00000497571.5:c.495G>C ENSP00000419923.1:p.Val165=
ENST00000542957.1:c.495G>C ENSP00000445301.1:p.Val165=
NM_001160124.1:c.495G>C NP_001153596.1:p.Val165=
NM_001160125.1:c.495G>C NP_001153597.1:p.Val165=
NM_001300.5:c.495G>C NP_001291.3:p.Val165=
NR_027653.1:n.762G>C
NM_001300.6:c.495G>C MANE Select NP_001291.3:p.Val165=
NM_001160124.2:c.495G>C NP_001153596.1:p.Val165=
NR_027653.2:n.690G>C
NM_001160125.2:c.495G>C NP_001153597.1:p.Val165=