Canonical Allele Identifier: CA345803382

Gene: KLF11

Linked Data

• ClinVar Variation Id: 1487596
• ClinVar RCV Id: RCV002008688
• dbSNP Id: rs2125279261
• MyVariant Identifiers: chr2:g.10188380C>A (hg19) ; chr2:g.10048253C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048253C>A , CM000664.2:g.10048253C>A	GRCh38
NC_000002.11:g.10188380C>A , CM000664.1:g.10188380C>A	GRCh37
NC_000002.10:g.10105831C>A	NCBI36
NG_017199.1:g.9699C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.916C>A MANE Select	ENSP00000307023.1:p.Pro306Thr
ENST00000305883.5:c.916C>A	ENSP00000307023.1:p.Pro306Thr
ENST00000535335.1:c.865C>A	ENSP00000442722.1:p.Pro289Thr
ENST00000540845.5:c.865C>A	ENSP00000444690.1:p.Pro289Thr
NM_001177716.1:c.865C>A	NP_001171187.1:p.Pro289Thr
NM_001177718.1:c.865C>A	NP_001171189.1:p.Pro289Thr
NM_003597.4:c.916C>A	NP_003588.1:p.Pro306Thr
XM_005246179.3:c.865C>A	XP_005246236.1:p.Pro289Thr
NM_003597.5:c.916C>A MANE Select	NP_003588.1:p.Pro306Thr
NM_001177716.2:c.865C>A	NP_001171187.1:p.Pro289Thr
NM_001177718.2:c.865C>A	NP_001171189.1:p.Pro289Thr