Canonical Allele Identifier: CA468166621
Gene: KLF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.3824146G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781954G>C , CM000672.2:g.3781954G>C GRCh38
NC_000010.10:g.3824146G>C , CM000672.1:g.3824146G>C GRCh37
NC_000010.9:g.3814146G>C NCBI36
NG_012277.1:g.8328C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.363C>G MANE Select ENSP00000419923.1:p.Pro121=
ENST00000173785.4:n.98C>G
ENST00000380946.3:n.598C>G
ENST00000469435.1:c.363C>G ENSP00000419079.1:p.Pro121=
ENST00000497571.5:c.363C>G ENSP00000419923.1:p.Pro121=
ENST00000542957.1:c.363C>G ENSP00000445301.1:p.Pro121=
NM_001160124.1:c.363C>G NP_001153596.1:p.Pro121=
NM_001160125.1:c.363C>G NP_001153597.1:p.Pro121=
NM_001300.5:c.363C>G NP_001291.3:p.Pro121=
NR_027653.1:n.630C>G
NM_001300.6:c.363C>G MANE Select NP_001291.3:p.Pro121=
NM_001160124.2:c.363C>G NP_001153596.1:p.Pro121=
NR_027653.2:n.558C>G
NM_001160125.2:c.363C>G NP_001153597.1:p.Pro121=