Canonical Allele Identifier: CA2488331434
Gene: KLF11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10048188_10048189delinsCT , CM000664.2:g.10048188_10048189delinsCT GRCh38
NC_000002.11:g.10188315_10188316delinsCT , CM000664.1:g.10188315_10188316delinsCT GRCh37
NC_000002.10:g.10105766_10105767delinsCT NCBI36
NG_017199.1:g.9634_9635delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000305883.6:c.851_852delinsCT MANE Select ENSP00000307023.1:p.Pro284=
ENST00000305883.5:c.851_852delinsCT ENSP00000307023.1:p.Pro284=
ENST00000535335.1:c.800_801delinsCT ENSP00000442722.1:p.Pro267=
ENST00000540845.5:c.800_801delinsCT ENSP00000444690.1:p.Pro267=
NM_001177716.1:c.800_801delinsCT NP_001171187.1:p.Pro267=
NM_001177718.1:c.800_801delinsCT NP_001171189.1:p.Pro267=
NM_003597.4:c.851_852delinsCT NP_003588.1:p.Pro284=
XM_005246179.3:c.800_801delinsCT XP_005246236.1:p.Pro267=
NM_003597.5:c.851_852delinsCT MANE Select NP_003588.1:p.Pro284=
NM_001177716.2:c.800_801delinsCT NP_001171187.1:p.Pro267=
NM_001177718.2:c.800_801delinsCT NP_001171189.1:p.Pro267=