Canonical Allele Identifier: CA345802819
Gene: KLF11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10048151A>C , CM000664.2:g.10048151A>C GRCh38
NC_000002.11:g.10188278A>C , CM000664.1:g.10188278A>C GRCh37
NC_000002.10:g.10105729A>C NCBI36
NG_017199.1:g.9597A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305883.6:c.814A>C MANE Select ENSP00000307023.1:p.Thr272Pro
ENST00000305883.5:c.814A>C ENSP00000307023.1:p.Thr272Pro
ENST00000535335.1:c.763A>C ENSP00000442722.1:p.Thr255Pro
ENST00000540845.5:c.763A>C ENSP00000444690.1:p.Thr255Pro
NM_001177716.1:c.763A>C NP_001171187.1:p.Thr255Pro
NM_001177718.1:c.763A>C NP_001171189.1:p.Thr255Pro
NM_003597.4:c.814A>C NP_003588.1:p.Thr272Pro
XM_005246179.3:c.763A>C XP_005246236.1:p.Thr255Pro
NM_003597.5:c.814A>C MANE Select NP_003588.1:p.Thr272Pro
NM_001177716.2:c.763A>C NP_001171187.1:p.Thr255Pro
NM_001177718.2:c.763A>C NP_001171189.1:p.Thr255Pro