Canonical Allele Identifier: CA1886882187
Gene: KLF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781705A= , CM000672.2:g.3781705A= GRCh38
NC_000010.10:g.3823897A= , CM000672.1:g.3823897A= GRCh37
NC_000010.9:g.3813897A= NCBI36
NG_012277.1:g.8577T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.612T= MANE Select ENSP00000419923.1:p.Phe204=
ENST00000173785.4:n.257+90T=
ENST00000469435.1:c.612T= ENSP00000419079.1:p.Phe204=
ENST00000497571.5:c.612T= ENSP00000419923.1:p.Phe204=
ENST00000542957.1:c.612T= ENSP00000445301.1:p.Phe204=
NM_001160124.1:c.550+62T= NP_001153596.1:n.550+62T=
NM_001160125.1:c.612T= NP_001153597.1:p.Phe204=
NM_001300.5:c.612T= NP_001291.3:p.Phe204=
NR_027653.1:n.789+90T=
NM_001300.6:c.612T= MANE Select NP_001291.3:p.Phe204=
NM_001160124.2:c.550+62T= NP_001153596.1:n.550+62T=
NR_027653.2:n.717+90T=
NM_001160125.2:c.612T= NP_001153597.1:p.Phe204=