Canonical Allele Identifier: CA345803001
Gene: KLF11 HGNC NCBI

Linked Data

dbSNP Id: rs1333165835
gnomAD v2: 2-10188299-T-C
gnomAD v4: 2-10048172-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10048172T>C , CM000664.2:g.10048172T>C GRCh38
NC_000002.11:g.10188299T>C , CM000664.1:g.10188299T>C GRCh37
NC_000002.10:g.10105750T>C NCBI36
NG_017199.1:g.9618T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305883.6:c.835T>C MANE Select ENSP00000307023.1:p.Ser279Pro
ENST00000305883.5:c.835T>C ENSP00000307023.1:p.Ser279Pro
ENST00000535335.1:c.784T>C ENSP00000442722.1:p.Ser262Pro
ENST00000540845.5:c.784T>C ENSP00000444690.1:p.Ser262Pro
NM_001177716.1:c.784T>C NP_001171187.1:p.Ser262Pro
NM_001177718.1:c.784T>C NP_001171189.1:p.Ser262Pro
NM_003597.4:c.835T>C NP_003588.1:p.Ser279Pro
XM_005246179.3:c.784T>C XP_005246236.1:p.Ser262Pro
NM_003597.5:c.835T>C MANE Select NP_003588.1:p.Ser279Pro
NM_001177716.2:c.784T>C NP_001171187.1:p.Ser262Pro
NM_001177718.2:c.784T>C NP_001171189.1:p.Ser262Pro