Canonical Allele Identifier: CA1886882179
Gene: KLF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781690T= , CM000672.2:g.3781690T= GRCh38
NC_000010.10:g.3823882T= , CM000672.1:g.3823882T= GRCh37
NC_000010.9:g.3813882T= NCBI36
NG_012277.1:g.8592A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.627A= MANE Select ENSP00000419923.1:p.Lys209=
ENST00000173785.4:n.257+105A=
ENST00000469435.1:c.627A= ENSP00000419079.1:p.Lys209=
ENST00000497571.5:c.627A= ENSP00000419923.1:p.Lys209=
ENST00000542957.1:c.627A= ENSP00000445301.1:p.Lys209=
NM_001160124.1:c.550+77A= NP_001153596.1:n.550+77A=
NM_001160125.1:c.627A= NP_001153597.1:p.Lys209=
NM_001300.5:c.627A= NP_001291.3:p.Lys209=
NR_027653.1:n.789+105A=
NM_001300.6:c.627A= MANE Select NP_001291.3:p.Lys209=
NM_001160124.2:c.550+77A= NP_001153596.1:n.550+77A=
NR_027653.2:n.717+105A=
NM_001160125.2:c.627A= NP_001153597.1:p.Lys209=