Canonical Allele Identifier: CA15840641
Gene: MEIS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.37050401T>C , CM000677.2:g.37050401T>C GRCh38
NC_000015.9:g.37342602T>C , CM000677.1:g.37342602T>C GRCh37
NC_000015.8:g.35129894T>C NCBI36
NG_029108.1:g.55899A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699903.1:c.716-13442A>G ENSP00000514679.1:n.716-13442A>G
ENST00000699904.1:c.716-13442A>G ENSP00000514680.1:n.716-13442A>G
ENST00000699905.1:n.429-13442A>G
ENST00000699955.1:c.755-13442A>G ENSP00000514715.1:n.755-13442A>G
ENST00000699956.1:c.317-13442A>G ENSP00000514716.1:n.317-13442A>G
ENST00000699957.1:n.415-13442A>G
ENST00000561208.6:c.755-13442A>G MANE Select ENSP00000453793.1:n.755-13442A>G
ENST00000314177.12:c.755-13442A>G ENSP00000326296.8:n.755-13442A>G
ENST00000338564.9:c.755-13442A>G ENSP00000341400.4:n.755-13442A>G
ENST00000340545.9:c.716-13442A>G ENSP00000339549.5:n.716-13442A>G
ENST00000397620.6:c.491-13442A>G ENSP00000380745.2:n.491-13442A>G
ENST00000397624.7:c.491-13442A>G ENSP00000380749.3:n.491-13442A>G
ENST00000424352.6:c.755-13442A>G ENSP00000404185.2:n.755-13442A>G
ENST00000557796.6:c.716-13442A>G ENSP00000452693.2:n.716-13442A>G
ENST00000559085.5:c.716-13442A>G ENSP00000453390.1:n.716-13442A>G
ENST00000559561.5:c.755-13442A>G ENSP00000453497.1:n.755-13442A>G
ENST00000560570.5:c.*316-13442A>G ENSP00000453481.1:n.*316-13442A>G
ENST00000561163.5:n.1075-13442A>G
ENST00000561208.5:c.755-13442A>G ENSP00000453793.1:n.755-13442A>G
ENST00000607277.5:c.332-13442A>G ENSP00000475899.1:n.332-13442A>G
NM_001220482.1:c.755-13442A>G NP_001207411.1:n.755-13442A>G
NM_002399.3:c.716-13442A>G NP_002390.1:n.716-13442A>G
NM_170674.4:c.755-13442A>G NP_733774.1:n.755-13442A>G
NM_170675.4:c.755-13442A>G NP_733775.1:n.755-13442A>G
NM_170676.4:c.755-13442A>G NP_733776.1:n.755-13442A>G
NM_170677.4:c.755-13442A>G NP_733777.1:n.755-13442A>G
NM_172315.2:c.716-13442A>G NP_758526.1:n.716-13442A>G
NM_172316.2:c.491-13442A>G NP_758527.1:n.491-13442A>G
NR_051953.1:n.1429-13442A>G
XM_006720522.2:c.755-13442A>G XP_006720585.1:n.755-13442A>G
XM_006720523.1:c.752-13442A>G XP_006720586.1:n.752-13442A>G
XM_006720524.1:c.752-13442A>G XP_006720587.1:n.752-13442A>G
XM_006720525.1:c.752-13442A>G XP_006720588.1:n.752-13442A>G
XM_006720526.2:c.491-13442A>G XP_006720589.1:n.491-13442A>G
XM_006720527.2:c.317-13442A>G XP_006720590.1:n.317-13442A>G
XM_006720528.2:c.317-13442A>G XP_006720591.1:n.317-13442A>G
XM_006720529.2:c.317-13442A>G XP_006720592.1:n.317-13442A>G
XM_011521591.1:c.317-13442A>G XP_011519893.1:n.317-13442A>G
XM_006720526.3:c.491-13442A>G XP_006720589.1:n.491-13442A>G
XM_006720527.3:c.317-13442A>G XP_006720590.1:n.317-13442A>G
XM_006720529.3:c.317-13442A>G XP_006720592.1:n.317-13442A>G
XM_011521591.2:c.317-13442A>G XP_011519893.1:n.317-13442A>G
XM_017022205.2:c.491-13442A>G XP_016877694.1:n.491-13442A>G
XM_024449925.1:c.716-13442A>G XP_024305693.1:n.716-13442A>G
XM_024449926.1:c.716-13442A>G XP_024305694.1:n.716-13442A>G
XM_024449927.1:c.716-13442A>G XP_024305695.1:n.716-13442A>G
XM_024449928.1:c.491-13442A>G XP_024305696.1:n.491-13442A>G
XM_024449929.1:c.716-13442A>G XP_024305697.1:n.716-13442A>G
XR_001751290.2:n.1190-13442A>G
XR_002957640.1:n.1143-13442A>G
XR_002957641.1:n.1143-13442A>G
NM_170675.5:c.755-13442A>G MANE Select NP_733775.1:n.755-13442A>G
NM_001220482.2:c.755-13442A>G NP_001207411.1:n.755-13442A>G
NM_170674.5:c.755-13442A>G NP_733774.1:n.755-13442A>G
NM_170676.5:c.755-13442A>G NP_733776.1:n.755-13442A>G
NM_170677.5:c.755-13442A>G NP_733777.1:n.755-13442A>G
NM_172315.3:c.716-13442A>G NP_758526.1:n.716-13442A>G
NR_051953.2:n.1838-13442A>G
NM_002399.4:c.716-13442A>G NP_002390.1:n.716-13442A>G
NM_172316.3:c.491-13442A>G NP_758527.1:n.491-13442A>G
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