Canonical Allele Identifier: CA1886882152
Gene: KLF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781620G= , CM000672.2:g.3781620G= GRCh38
NC_000010.10:g.3823812G= , CM000672.1:g.3823812G= GRCh37
NC_000010.9:g.3813812G= NCBI36
NG_012277.1:g.8662C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.676+21C= MANE Select ENSP00000419923.1:n.676+21C=
ENST00000173785.4:n.257+175C=
ENST00000469435.1:c.697C= ENSP00000419079.1:p.Arg233=
ENST00000497571.5:c.676+21C= ENSP00000419923.1:n.676+21C=
ENST00000542957.1:c.676+21C= ENSP00000445301.1:n.676+21C=
NM_001160124.1:c.550+147C= NP_001153596.1:n.550+147C=
NM_001160125.1:c.676+21C= NP_001153597.1:n.676+21C=
NM_001300.5:c.676+21C= NP_001291.3:n.676+21C=
NR_027653.1:n.789+175C=
NM_001300.6:c.676+21C= MANE Select NP_001291.3:n.676+21C=
NM_001160124.2:c.550+147C= NP_001153596.1:n.550+147C=
NR_027653.2:n.717+175C=
NM_001160125.2:c.676+21C= NP_001153597.1:n.676+21C=