Canonical Allele Identifier: CA617561213
Gene: MEIS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.37098113dup , CM000677.2:g.37098113dup GRCh38
NC_000015.9:g.37390314dup , CM000677.1:g.37390314dup GRCh37
NC_000015.8:g.35177606dup NCBI36
NG_029108.1:g.8192dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000699903.1:c.65dup ENSP00000514679.1:p.Val23GlyfsTer?
ENST00000699904.1:c.65dup ENSP00000514680.1:p.Val23GlyfsTer?
ENST00000699955.1:c.104dup ENSP00000514715.1:p.Val36GlyfsTer?
ENST00000561208.6:c.104dup MANE Select ENSP00000453793.1:p.Val36GlyfsTer?
ENST00000314177.12:c.104dup ENSP00000326296.8:p.Val36GlyfsTer?
ENST00000338564.9:c.104dup ENSP00000341400.4:p.Val36GlyfsTer?
ENST00000340545.9:c.65dup ENSP00000339549.5:p.Val23GlyfsTer?
ENST00000397620.6:c.-138dup ENSP00000380745.2:n.-138dup
ENST00000397624.7:c.-138dup ENSP00000380749.3:n.-138dup
ENST00000424352.6:c.104dup ENSP00000404185.2:p.Val36GlyfsTer?
ENST00000557796.6:c.65dup ENSP00000452693.2:p.Val23GlyfsTer?
ENST00000558313.5:c.-138dup ENSP00000453782.2:n.-138dup
ENST00000559085.5:c.65dup ENSP00000453390.1:p.Val23GlyfsTer?
ENST00000559561.5:c.104dup ENSP00000453497.1:p.Val36GlyfsTer?
ENST00000560570.5:c.104dup ENSP00000453481.1:p.Val36GlyfsTer?
ENST00000561163.5:n.424dup
ENST00000561208.5:c.104dup ENSP00000453793.1:p.Val36GlyfsTer?
NM_001220482.1:c.104dup NP_001207411.1:p.Val36GlyfsTer?
NM_002399.3:c.65dup NP_002390.1:p.Val23GlyfsTer?
NM_170674.4:c.104dup NP_733774.1:p.Val36GlyfsTer?
NM_170675.4:c.104dup NP_733775.1:p.Val36GlyfsTer?
NM_170676.4:c.104dup NP_733776.1:p.Val36GlyfsTer?
NM_170677.4:c.104dup NP_733777.1:p.Val36GlyfsTer?
NM_172315.2:c.65dup NP_758526.1:p.Val23GlyfsTer?
NM_172316.2:c.-138dup NP_758527.1:n.-138dup
NR_051953.1:n.778dup
XM_006720522.2:c.104dup XP_006720585.1:p.Val36GlyfsTer?
XM_006720523.1:c.101dup XP_006720586.1:p.Val35GlyfsTer?
XM_006720524.1:c.101dup XP_006720587.1:p.Val35GlyfsTer?
XM_006720525.1:c.101dup XP_006720588.1:p.Val35GlyfsTer?
XM_006720526.2:c.-138dup XP_006720589.1:n.-138dup
XM_006720527.2:c.-193dup XP_006720590.1:n.-193dup
XM_006720528.2:c.-51-2494dup XP_006720591.1:n.-51-2494dup
XM_006720529.2:c.-193dup XP_006720592.1:n.-193dup
XM_006720526.3:c.-138dup XP_006720589.1:n.-138dup
XM_006720527.3:c.-193dup XP_006720590.1:n.-193dup
XM_006720529.3:c.-193dup XP_006720592.1:n.-193dup
XM_017022205.2:c.-138dup XP_016877694.1:n.-138dup
XM_024449925.1:c.65dup XP_024305693.1:p.Val23GlyfsTer?
XM_024449926.1:c.65dup XP_024305694.1:p.Val23GlyfsTer?
XM_024449927.1:c.65dup XP_024305695.1:p.Val23GlyfsTer?
XM_024449928.1:c.-138dup XP_024305696.1:n.-138dup
XM_024449929.1:c.65dup XP_024305697.1:p.Val23GlyfsTer?
XR_001751290.2:n.539dup
XR_002957640.1:n.492dup
XR_002957641.1:n.492dup
NM_170675.5:c.104dup MANE Select NP_733775.1:p.Val36GlyfsTer?
NM_001220482.2:c.104dup NP_001207411.1:p.Val36GlyfsTer?
NM_170674.5:c.104dup NP_733774.1:p.Val36GlyfsTer?
NM_170676.5:c.104dup NP_733776.1:p.Val36GlyfsTer?
NM_170677.5:c.104dup NP_733777.1:p.Val36GlyfsTer?
NM_172315.3:c.65dup NP_758526.1:p.Val23GlyfsTer?
NR_051953.2:n.1187dup
NM_002399.4:c.65dup NP_002390.1:p.Val23GlyfsTer?
NM_172316.3:c.-138dup NP_758527.1:n.-138dup