Canonical Allele Identifier: CA425084839
Gene: KLF11 HGNC NCBI

Linked Data

dbSNP Id: rs1386870459
gnomAD v3: 2-10048168-T-G
gnomAD v4: 2-10048168-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10048168T>G , CM000664.2:g.10048168T>G GRCh38
NC_000002.11:g.10188295T>G , CM000664.1:g.10188295T>G GRCh37
NC_000002.10:g.10105746T>G NCBI36
NG_017199.1:g.9614T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000305883.6:c.831T>G MANE Select ENSP00000307023.1:p.Ser277=
ENST00000305883.5:c.831T>G ENSP00000307023.1:p.Ser277=
ENST00000535335.1:c.780T>G ENSP00000442722.1:p.Ser260=
ENST00000540845.5:c.780T>G ENSP00000444690.1:p.Ser260=
NM_001177716.1:c.780T>G NP_001171187.1:p.Ser260=
NM_001177718.1:c.780T>G NP_001171189.1:p.Ser260=
NM_003597.4:c.831T>G NP_003588.1:p.Ser277=
XM_005246179.3:c.780T>G XP_005246236.1:p.Ser260=
NM_003597.5:c.831T>G MANE Select NP_003588.1:p.Ser277=
NM_001177716.2:c.780T>G NP_001171187.1:p.Ser260=
NM_001177718.2:c.780T>G NP_001171189.1:p.Ser260=