Canonical Allele Identifier: CA16619921
Gene: MEIS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418712
dbSNP Id: rs1064793383

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.36950396G>A , CM000677.2:g.36950396G>A GRCh38
NC_000015.9:g.37242597G>A , CM000677.1:g.37242597G>A GRCh37
NC_000015.8:g.35029889G>A NCBI36
NG_029108.1:g.155904C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000699898.1:n.88C>T
ENST00000699899.1:n.88C>T
ENST00000699900.1:n.138C>T
ENST00000699901.1:n.228C>T
ENST00000699902.1:n.68C>T
ENST00000699903.1:c.866C>T ENSP00000514679.1:p.Pro289Leu
ENST00000699904.1:c.866C>T ENSP00000514680.1:p.Pro289Leu
ENST00000699905.1:n.579C>T
ENST00000699955.1:c.*116C>T ENSP00000514715.1:n.*116C>T
ENST00000699956.1:c.467C>T ENSP00000514716.1:p.Pro156Leu
ENST00000561208.6:c.905C>T MANE Select ENSP00000453793.1:p.Pro302Leu
ENST00000314177.12:c.901-53710C>T ENSP00000326296.8:n.901-53710C>T
ENST00000338564.9:c.905C>T ENSP00000341400.4:p.Pro302Leu
ENST00000340545.9:c.866C>T ENSP00000339549.5:p.Pro289Leu
ENST00000397620.6:c.641C>T ENSP00000380745.2:p.Pro214Leu
ENST00000397624.7:c.641C>T ENSP00000380749.3:p.Pro214Leu
ENST00000424352.6:c.905C>T ENSP00000404185.2:p.Pro302Leu
ENST00000557796.6:c.866C>T ENSP00000452693.2:p.Pro289Leu
ENST00000559085.5:c.866C>T ENSP00000453390.1:p.Pro289Leu
ENST00000559561.5:c.905C>T ENSP00000453497.1:p.Pro302Leu
ENST00000560570.5:c.*466C>T ENSP00000453481.1:n.*466C>T
ENST00000561208.5:c.905C>T ENSP00000453793.1:p.Pro302Leu
ENST00000607277.5:c.482C>T ENSP00000475899.1:p.Pro161Leu
NM_001220482.1:c.905C>T NP_001207411.1:p.Pro302Leu
NM_002399.3:c.866C>T NP_002390.1:p.Pro289Leu
NM_170674.4:c.905C>T NP_733774.1:p.Pro302Leu
NM_170675.4:c.905C>T NP_733775.1:p.Pro302Leu
NM_170676.4:c.905C>T NP_733776.1:p.Pro302Leu
NM_170677.4:c.905C>T NP_733777.1:p.Pro302Leu
NM_172315.2:c.866C>T NP_758526.1:p.Pro289Leu
NM_172316.2:c.641C>T NP_758527.1:p.Pro214Leu
NR_051953.1:n.1575-53710C>T
XM_006720522.2:c.905C>T XP_006720585.1:p.Pro302Leu
XM_006720523.1:c.902C>T XP_006720586.1:p.Pro301Leu
XM_006720524.1:c.902C>T XP_006720587.1:p.Pro301Leu
XM_006720525.1:c.902C>T XP_006720588.1:p.Pro301Leu
XM_006720526.2:c.641C>T XP_006720589.1:p.Pro214Leu
XM_006720527.2:c.467C>T XP_006720590.1:p.Pro156Leu
XM_006720528.2:c.467C>T XP_006720591.1:p.Pro156Leu
XM_006720529.2:c.467C>T XP_006720592.1:p.Pro156Leu
XM_011521591.1:c.467C>T XP_011519893.1:p.Pro156Leu
XM_006720526.3:c.641C>T XP_006720589.1:p.Pro214Leu
XM_006720527.3:c.467C>T XP_006720590.1:p.Pro156Leu
XM_006720529.3:c.467C>T XP_006720592.1:p.Pro156Leu
XM_011521591.2:c.467C>T XP_011519893.1:p.Pro156Leu
XM_017022205.2:c.641C>T XP_016877694.1:p.Pro214Leu
XM_024449925.1:c.866C>T XP_024305693.1:p.Pro289Leu
XM_024449926.1:c.866C>T XP_024305694.1:p.Pro289Leu
XM_024449927.1:c.866C>T XP_024305695.1:p.Pro289Leu
XM_024449928.1:c.641C>T XP_024305696.1:p.Pro214Leu
XM_024449929.1:c.866C>T XP_024305697.1:p.Pro289Leu
XR_001751290.2:n.1336-53710C>T
XR_002957640.1:n.1289-53710C>T
XR_002957641.1:n.1289-53710C>T
NM_170675.5:c.905C>T MANE Select NP_733775.1:p.Pro302Leu
NM_001220482.2:c.905C>T NP_001207411.1:p.Pro302Leu
NM_170674.5:c.905C>T NP_733774.1:p.Pro302Leu
NM_170676.5:c.905C>T NP_733776.1:p.Pro302Leu
NM_170677.5:c.905C>T NP_733777.1:p.Pro302Leu
NM_172315.3:c.866C>T NP_758526.1:p.Pro289Leu
NR_051953.2:n.1984-53710C>T
NM_002399.4:c.866C>T NP_002390.1:p.Pro289Leu
NM_172316.3:c.641C>T NP_758527.1:p.Pro214Leu