Canonical Allele Identifier: CA1886882269
Gene: KLF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781884T= , CM000672.2:g.3781884T= GRCh38
NC_000010.10:g.3824076T= , CM000672.1:g.3824076T= GRCh37
NC_000010.9:g.3814076T= NCBI36
NG_012277.1:g.8398A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.433A= MANE Select ENSP00000419923.1:p.Thr145=
ENST00000173785.4:n.168A=
ENST00000380946.3:n.668A=
ENST00000469435.1:c.433A= ENSP00000419079.1:p.Thr145=
ENST00000497571.5:c.433A= ENSP00000419923.1:p.Thr145=
ENST00000542957.1:c.433A= ENSP00000445301.1:p.Thr145=
NM_001160124.1:c.433A= NP_001153596.1:p.Thr145=
NM_001160125.1:c.433A= NP_001153597.1:p.Thr145=
NM_001300.5:c.433A= NP_001291.3:p.Thr145=
NR_027653.1:n.700A=
NM_001300.6:c.433A= MANE Select NP_001291.3:p.Thr145=
NM_001160124.2:c.433A= NP_001153596.1:p.Thr145=
NR_027653.2:n.628A=
NM_001160125.2:c.433A= NP_001153597.1:p.Thr145=