Canonical Allele Identifier: CA16619920
Gene: MEIS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423971
ClinVar RCV Id: RCV000487166
dbSNP Id: rs1064796723

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.36950336T>A , CM000677.2:g.36950336T>A GRCh38
NC_000015.9:g.37242537T>A , CM000677.1:g.37242537T>A GRCh37
NC_000015.8:g.35029829T>A NCBI36
NG_029108.1:g.155964A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000699898.1:n.148A>T
ENST00000699899.1:n.148A>T
ENST00000699900.1:n.198A>T
ENST00000699901.1:n.288A>T
ENST00000699902.1:n.128A>T
ENST00000699903.1:c.926A>T ENSP00000514679.1:p.Gln309Leu
ENST00000699904.1:c.926A>T ENSP00000514680.1:p.Gln309Leu
ENST00000699905.1:n.639A>T
ENST00000699955.1:c.*176A>T ENSP00000514715.1:n.*176A>T
ENST00000699956.1:c.527A>T ENSP00000514716.1:p.Gln176Leu
ENST00000561208.6:c.965A>T MANE Select ENSP00000453793.1:p.Gln322Leu
ENST00000314177.12:c.901-53650A>T ENSP00000326296.8:n.901-53650A>T
ENST00000338564.9:c.965A>T ENSP00000341400.4:p.Gln322Leu
ENST00000340545.9:c.926A>T ENSP00000339549.5:p.Gln309Leu
ENST00000397620.6:c.701A>T ENSP00000380745.2:p.Gln234Leu
ENST00000397624.7:c.701A>T ENSP00000380749.3:p.Gln234Leu
ENST00000424352.6:c.965A>T ENSP00000404185.2:p.Gln322Leu
ENST00000557796.6:c.926A>T ENSP00000452693.2:p.Gln309Leu
ENST00000559085.5:c.926A>T ENSP00000453390.1:p.Gln309Leu
ENST00000559561.5:c.965A>T ENSP00000453497.1:p.Gln322Leu
ENST00000560570.5:c.*526A>T ENSP00000453481.1:n.*526A>T
ENST00000561208.5:c.965A>T ENSP00000453793.1:p.Gln322Leu
ENST00000607277.5:c.542A>T ENSP00000475899.1:p.Gln181Leu
NM_001220482.1:c.965A>T NP_001207411.1:p.Gln322Leu
NM_002399.3:c.926A>T NP_002390.1:p.Gln309Leu
NM_170674.4:c.965A>T NP_733774.1:p.Gln322Leu
NM_170675.4:c.965A>T NP_733775.1:p.Gln322Leu
NM_170676.4:c.965A>T NP_733776.1:p.Gln322Leu
NM_170677.4:c.965A>T NP_733777.1:p.Gln322Leu
NM_172315.2:c.926A>T NP_758526.1:p.Gln309Leu
NM_172316.2:c.701A>T NP_758527.1:p.Gln234Leu
NR_051953.1:n.1575-53650A>T
XM_006720522.2:c.965A>T XP_006720585.1:p.Gln322Leu
XM_006720523.1:c.962A>T XP_006720586.1:p.Gln321Leu
XM_006720524.1:c.962A>T XP_006720587.1:p.Gln321Leu
XM_006720525.1:c.962A>T XP_006720588.1:p.Gln321Leu
XM_006720526.2:c.701A>T XP_006720589.1:p.Gln234Leu
XM_006720527.2:c.527A>T XP_006720590.1:p.Gln176Leu
XM_006720528.2:c.527A>T XP_006720591.1:p.Gln176Leu
XM_006720529.2:c.527A>T XP_006720592.1:p.Gln176Leu
XM_011521591.1:c.527A>T XP_011519893.1:p.Gln176Leu
XM_006720526.3:c.701A>T XP_006720589.1:p.Gln234Leu
XM_006720527.3:c.527A>T XP_006720590.1:p.Gln176Leu
XM_006720529.3:c.527A>T XP_006720592.1:p.Gln176Leu
XM_011521591.2:c.527A>T XP_011519893.1:p.Gln176Leu
XM_017022205.2:c.701A>T XP_016877694.1:p.Gln234Leu
XM_024449925.1:c.926A>T XP_024305693.1:p.Gln309Leu
XM_024449926.1:c.926A>T XP_024305694.1:p.Gln309Leu
XM_024449927.1:c.926A>T XP_024305695.1:p.Gln309Leu
XM_024449928.1:c.701A>T XP_024305696.1:p.Gln234Leu
XM_024449929.1:c.926A>T XP_024305697.1:p.Gln309Leu
XR_001751290.2:n.1336-53650A>T
XR_002957640.1:n.1289-53650A>T
XR_002957641.1:n.1289-53650A>T
NM_170675.5:c.965A>T MANE Select NP_733775.1:p.Gln322Leu
NM_001220482.2:c.965A>T NP_001207411.1:p.Gln322Leu
NM_170674.5:c.965A>T NP_733774.1:p.Gln322Leu
NM_170676.5:c.965A>T NP_733776.1:p.Gln322Leu
NM_170677.5:c.965A>T NP_733777.1:p.Gln322Leu
NM_172315.3:c.926A>T NP_758526.1:p.Gln309Leu
NR_051953.2:n.1984-53650A>T
NM_002399.4:c.926A>T NP_002390.1:p.Gln309Leu
NM_172316.3:c.701A>T NP_758527.1:p.Gln234Leu