Canonical Allele Identifier: CA1886882291
Gene: KLF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781928A= , CM000672.2:g.3781928A= GRCh38
NC_000010.10:g.3824120A= , CM000672.1:g.3824120A= GRCh37
NC_000010.9:g.3814120A= NCBI36
NG_012277.1:g.8354T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.389T= MANE Select ENSP00000419923.1:p.Ile130=
ENST00000173785.4:n.124T=
ENST00000380946.3:n.624T=
ENST00000469435.1:c.389T= ENSP00000419079.1:p.Ile130=
ENST00000497571.5:c.389T= ENSP00000419923.1:p.Ile130=
ENST00000542957.1:c.389T= ENSP00000445301.1:p.Ile130=
NM_001160124.1:c.389T= NP_001153596.1:p.Ile130=
NM_001160125.1:c.389T= NP_001153597.1:p.Ile130=
NM_001300.5:c.389T= NP_001291.3:p.Ile130=
NR_027653.1:n.656T=
NM_001300.6:c.389T= MANE Select NP_001291.3:p.Ile130=
NM_001160124.2:c.389T= NP_001153596.1:p.Ile130=
NR_027653.2:n.584T=
NM_001160125.2:c.389T= NP_001153597.1:p.Ile130=