Canonical Allele Identifier: CA230452225

Gene: PKNOX2

Linked Data

• dbSNP Id: rs1026803554
• MyVariant Identifiers: chr11:g.125240879G>T (hg19) ; chr11:g.125370983G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.125370983G>T , CM000673.2:g.125370983G>T	GRCh38
NC_000011.9:g.125240879G>T , CM000673.1:g.125240879G>T	GRCh37
NC_000011.8:g.124746089G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298282.14:c.227+2998G>T MANE Select	ENSP00000298282.8:n.227+2998G>T
ENST00000298282.13:c.227+2998G>T	ENSP00000298282.8:n.227+2998G>T
ENST00000530517.5:n.408+2998G>T
ENST00000531116.5:n.329+2998G>T
ENST00000532623.5:c.88-14568G>T	ENSP00000434377.1:n.88-14568G>T
ENST00000557814.5:n.369+2998G>T
ENST00000558705.1:c.227+2998G>T	ENSP00000453374.1:n.227+2998G>T
ENST00000558729.5:n.562+2998G>T
ENST00000559662.5:n.478+2998G>T
ENST00000561298.1:n.453+2998G>T
NM_022062.2:c.227+2998G>T	NP_071345.2:n.227+2998G>T
XM_005271642.1:c.227+2998G>T	XP_005271699.1:n.227+2998G>T
XM_005271643.1:c.140+2998G>T	XP_005271700.1:n.140+2998G>T
XM_006718894.1:c.-1+2998G>T	XP_006718957.1:n.-1+2998G>T
XM_011542944.1:c.227+2998G>T	XP_011541246.1:n.227+2998G>T
XM_011542945.1:c.227+2998G>T	XP_011541247.1:n.227+2998G>T
XM_011542946.1:c.227+2998G>T	XP_011541248.1:n.227+2998G>T
XM_011542947.1:c.-1+2998G>T	XP_011541249.1:n.-1+2998G>T
XM_005271642.2:c.227+2998G>T	XP_005271699.1:n.227+2998G>T
XM_006718894.2:c.-1+2998G>T	XP_006718957.1:n.-1+2998G>T
XM_011542945.2:c.227+2998G>T	XP_011541247.1:n.227+2998G>T
XM_011542947.2:c.-1+2998G>T	XP_011541249.1:n.-1+2998G>T
XM_017018110.1:c.227+2998G>T	XP_016873599.1:n.227+2998G>T
XM_017018111.1:c.-1+2998G>T	XP_016873600.1:n.-1+2998G>T
XM_024448643.1:c.227+2998G>T	XP_024304411.1:n.227+2998G>T
XM_024448644.1:c.227+2998G>T	XP_024304412.1:n.227+2998G>T
XM_024448645.1:c.227+2998G>T	XP_024304413.1:n.227+2998G>T
XM_024448646.1:c.227+2998G>T	XP_024304414.1:n.227+2998G>T
XM_024448647.1:c.227+2998G>T	XP_024304415.1:n.227+2998G>T
XM_024448648.1:c.140+2998G>T	XP_024304416.1:n.140+2998G>T
XM_024448649.1:c.140+2998G>T	XP_024304417.1:n.140+2998G>T
XM_024448650.1:c.140+2998G>T	XP_024304418.1:n.140+2998G>T
XM_024448651.1:c.140+2998G>T	XP_024304419.1:n.140+2998G>T
NM_022062.3:c.227+2998G>T	NP_071345.2:n.227+2998G>T
NM_001382323.2:c.227+2998G>T MANE Select	NP_001369252.1:n.227+2998G>T
NM_001382324.1:c.227+2998G>T	NP_001369253.1:n.227+2998G>T
NM_001382325.1:c.227+2998G>T	NP_001369254.1:n.227+2998G>T
NM_001382326.1:c.227+2998G>T	NP_001369255.1:n.227+2998G>T
NM_001382327.1:c.227+2998G>T	NP_001369256.1:n.227+2998G>T
NM_001382328.1:c.227+2998G>T	NP_001369257.1:n.227+2998G>T
NM_001382329.1:c.140+2998G>T	NP_001369258.1:n.140+2998G>T
NM_001382330.1:c.140+2998G>T	NP_001369259.1:n.140+2998G>T
NM_001382331.1:c.140+2998G>T	NP_001369260.1:n.140+2998G>T
NM_001382332.1:c.140+2998G>T	NP_001369261.1:n.140+2998G>T
NM_001382333.1:c.140+2998G>T	NP_001369262.1:n.140+2998G>T
NM_001382334.1:c.227+2998G>T	NP_001369263.1:n.227+2998G>T
NM_001382335.1:c.227+2998G>T	NP_001369264.1:n.227+2998G>T
NM_001382336.1:c.140+2998G>T	NP_001369265.1:n.140+2998G>T
NM_001382337.1:c.140+2998G>T	NP_001369266.1:n.140+2998G>T
NM_001382338.1:c.140+2998G>T	NP_001369267.1:n.140+2998G>T
NM_001382339.1:c.227+2998G>T	NP_001369268.1:n.227+2998G>T
NM_001382340.1:c.36-14568G>T	NP_001369269.1:n.36-14568G>T
NM_001382341.1:c.227+2998G>T	NP_001369270.1:n.227+2998G>T
NR_168076.1:n.344+2998G>T
NR_168077.1:n.275+2998G>T
NR_168078.1:n.453+2998G>T
NR_168079.1:n.453+2998G>T
NR_168080.1:n.455+2998G>T
NR_168081.1:n.382+2998G>T
NR_168082.1:n.526+2998G>T
NR_168083.1:n.453+2998G>T
NR_168084.1:n.382+2998G>T