Canonical Allele Identifier: CA1886882171
Gene: KLF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781660T= , CM000672.2:g.3781660T= GRCh38
NC_000010.10:g.3823852T= , CM000672.1:g.3823852T= GRCh37
NC_000010.9:g.3813852T= NCBI36
NG_012277.1:g.8622A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.657A= MANE Select ENSP00000419923.1:p.Ala219=
ENST00000173785.4:n.257+135A=
ENST00000469435.1:c.657A= ENSP00000419079.1:p.Ala219=
ENST00000497571.5:c.657A= ENSP00000419923.1:p.Ala219=
ENST00000542957.1:c.657A= ENSP00000445301.1:p.Ala219=
NM_001160124.1:c.550+107A= NP_001153596.1:n.550+107A=
NM_001160125.1:c.657A= NP_001153597.1:p.Ala219=
NM_001300.5:c.657A= NP_001291.3:p.Ala219=
NR_027653.1:n.789+135A=
NM_001300.6:c.657A= MANE Select NP_001291.3:p.Ala219=
NM_001160124.2:c.550+107A= NP_001153596.1:n.550+107A=
NR_027653.2:n.717+135A=
NM_001160125.2:c.657A= NP_001153597.1:p.Ala219=