Canonical Allele Identifier: CA345803279
Gene: KLF11 HGNC NCBI

Linked Data

dbSNP Id: rs1367443811

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10048224G>C , CM000664.2:g.10048224G>C GRCh38
NC_000002.11:g.10188351G>C , CM000664.1:g.10188351G>C GRCh37
NC_000002.10:g.10105802G>C NCBI36
NG_017199.1:g.9670G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305883.6:c.887G>C MANE Select ENSP00000307023.1:p.Ser296Thr
ENST00000305883.5:c.887G>C ENSP00000307023.1:p.Ser296Thr
ENST00000535335.1:c.836G>C ENSP00000442722.1:p.Ser279Thr
ENST00000540845.5:c.836G>C ENSP00000444690.1:p.Ser279Thr
NM_001177716.1:c.836G>C NP_001171187.1:p.Ser279Thr
NM_001177718.1:c.836G>C NP_001171189.1:p.Ser279Thr
NM_003597.4:c.887G>C NP_003588.1:p.Ser296Thr
XM_005246179.3:c.836G>C XP_005246236.1:p.Ser279Thr
NM_003597.5:c.887G>C MANE Select NP_003588.1:p.Ser296Thr
NM_001177716.2:c.836G>C NP_001171187.1:p.Ser279Thr
NM_001177718.2:c.836G>C NP_001171189.1:p.Ser279Thr