Canonical Allele Identifier: CA230346078

Gene: PKNOX2

Linked Data

• dbSNP Id: rs1022527465
• gnomAD v3: 11-125308652-G-A
• gnomAD v4: 11-125308652-G-A
• MyVariant Identifiers: chr11:g.125178548G>A (hg19) ; chr11:g.125308652G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.125308652G>A , CM000673.2:g.125308652G>A	GRCh38
NC_000011.9:g.125178548G>A , CM000673.1:g.125178548G>A	GRCh37
NC_000011.8:g.124683758G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298282.14:c.-129-23167G>A MANE Select	ENSP00000298282.8:n.-129-23167G>A
ENST00000298282.13:c.-129-23167G>A	ENSP00000298282.8:n.-129-23167G>A
ENST00000527238.5:c.-202-23167G>A	ENSP00000431599.1:n.-202-23167G>A
ENST00000530517.5:n.162-23167G>A
ENST00000531116.5:n.83-23167G>A
ENST00000531212.5:c.-129-23167G>A	ENSP00000434255.1:n.-129-23167G>A
ENST00000532623.5:c.-129-23167G>A	ENSP00000434377.1:n.-129-23167G>A
ENST00000557814.5:n.121-42632G>A
ENST00000558729.5:n.207-23167G>A
ENST00000559662.5:n.123-23167G>A
ENST00000561115.5:n.197-23167G>A
NM_022062.2:c.-129-23167G>A	NP_071345.2:n.-129-23167G>A
XM_005271642.1:c.-129-23167G>A	XP_005271699.1:n.-129-23167G>A
XM_006718894.1:c.-356-23167G>A	XP_006718957.1:n.-356-23167G>A
XM_011542944.1:c.-129-23167G>A	XP_011541246.1:n.-129-23167G>A
XM_011542945.1:c.-202-23167G>A	XP_011541247.1:n.-202-23167G>A
XM_011542946.1:c.-129-23167G>A	XP_011541248.1:n.-129-23167G>A
XM_011542947.1:c.-249-42632G>A	XP_011541249.1:n.-249-42632G>A
XM_005271642.2:c.-129-23167G>A	XP_005271699.1:n.-129-23167G>A
XM_006718894.2:c.-356-23167G>A	XP_006718957.1:n.-356-23167G>A
XM_011542945.2:c.-202-23167G>A	XP_011541247.1:n.-202-23167G>A
XM_011542947.2:c.-249-42632G>A	XP_011541249.1:n.-249-42632G>A
XM_017018110.1:c.-129-23167G>A	XP_016873599.1:n.-129-23167G>A
XM_017018111.1:c.-247-23167G>A	XP_016873600.1:n.-247-23167G>A
XM_024448643.1:c.-129-23167G>A	XP_024304411.1:n.-129-23167G>A
XM_024448644.1:c.-129-23167G>A	XP_024304412.1:n.-129-23167G>A
XM_024448645.1:c.-129-23167G>A	XP_024304413.1:n.-129-23167G>A
XM_024448646.1:c.-202-23167G>A	XP_024304414.1:n.-202-23167G>A
XM_024448647.1:c.-22-42632G>A	XP_024304415.1:n.-22-42632G>A
XM_024448648.1:c.-107-23167G>A	XP_024304416.1:n.-107-23167G>A
XM_024448649.1:c.-107-23167G>A	XP_024304417.1:n.-107-23167G>A
XM_024448650.1:c.-107-23167G>A	XP_024304418.1:n.-107-23167G>A
XM_024448651.1:c.-107-23167G>A	XP_024304419.1:n.-107-23167G>A
NM_022062.3:c.-129-23167G>A	NP_071345.2:n.-129-23167G>A
NM_001382323.2:c.-129-23167G>A MANE Select	NP_001369252.1:n.-129-23167G>A
NM_001382324.1:c.-202-23167G>A	NP_001369253.1:n.-202-23167G>A
NM_001382325.1:c.-22-42632G>A	NP_001369254.1:n.-22-42632G>A
NM_001382326.1:c.-202-23167G>A	NP_001369255.1:n.-202-23167G>A
NM_001382327.1:c.-129-23167G>A	NP_001369256.1:n.-129-23167G>A
NM_001382328.1:c.-129-23167G>A	NP_001369257.1:n.-129-23167G>A
NM_001382329.1:c.1-59194G>A	NP_001369258.1:n.1-59194G>A
NM_001382330.1:c.-107-23167G>A	NP_001369259.1:n.-107-23167G>A
NM_001382331.1:c.-107-23167G>A	NP_001369260.1:n.-107-23167G>A
NM_001382332.1:c.-107-23167G>A	NP_001369261.1:n.-107-23167G>A
NM_001382333.1:c.-107-23167G>A	NP_001369262.1:n.-107-23167G>A
NM_001382334.1:c.-129-23167G>A	NP_001369263.1:n.-129-23167G>A
NM_001382335.1:c.-129-23167G>A	NP_001369264.1:n.-129-23167G>A
NM_001382336.1:c.-107-23167G>A	NP_001369265.1:n.-107-23167G>A
NM_001382337.1:c.-107-23167G>A	NP_001369266.1:n.-107-23167G>A
NM_001382338.1:c.1-59194G>A	NP_001369267.1:n.1-59194G>A
NM_001382339.1:c.-129-23167G>A	NP_001369268.1:n.-129-23167G>A
NM_001382340.1:c.-181-23167G>A	NP_001369269.1:n.-181-23167G>A
NM_001382341.1:c.-129-23167G>A	NP_001369270.1:n.-129-23167G>A
NR_168076.1:n.98-23167G>A
NR_168077.1:n.27-42632G>A
NR_168078.1:n.98-23167G>A
NR_168079.1:n.98-23167G>A
NR_168080.1:n.27-23167G>A
NR_168081.1:n.27-23167G>A
NR_168082.1:n.98-23167G>A
NR_168083.1:n.98-23167G>A
NR_168084.1:n.27-23167G>A