Canonical Allele Identifier: CA2170135719
Gene: MEIS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.36896636T= , CM000677.2:g.36896636T= GRCh38
NC_000015.9:g.37188837T= , CM000677.1:g.37188837T= GRCh37
NC_000015.8:g.34976129T= NCBI36
NG_029108.1:g.209664A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699898.1:n.211A=
ENST00000699899.1:n.211A=
ENST00000699900.1:n.261A=
ENST00000699901.1:n.351A=
ENST00000699902.1:n.191A=
ENST00000699903.1:c.989A= ENSP00000514679.1:p.Asn330=
ENST00000699904.1:c.1130A= ENSP00000514680.1:p.Asn377=
ENST00000699905.1:n.702A=
ENST00000699906.1:n.255A=
ENST00000699955.1:c.*239A= ENSP00000514715.1:n.*239A=
ENST00000699956.1:c.590A= ENSP00000514716.1:p.Asn197=
ENST00000561208.6:c.1028A= MANE Select ENSP00000453793.1:p.Asn343=
ENST00000314177.12:c.*42A= ENSP00000326296.8:n.*42A=
ENST00000338564.9:c.1028A= ENSP00000341400.4:p.Asn343=
ENST00000340545.9:c.989A= ENSP00000339549.5:p.Asn330=
ENST00000397620.6:c.764A= ENSP00000380745.2:p.Asn255=
ENST00000397624.7:c.764A= ENSP00000380749.3:p.Asn255=
ENST00000424352.6:c.1028A= ENSP00000404185.2:p.Asn343=
ENST00000557796.6:c.989A= ENSP00000452693.2:p.Asn330=
ENST00000558643.1:n.515A=
ENST00000559085.5:c.989A= ENSP00000453390.1:p.Asn330=
ENST00000559371.5:n.357+84A=
ENST00000559408.1:n.434A=
ENST00000559561.5:c.1028A= ENSP00000453497.1:p.Asn343=
ENST00000560570.5:c.*589A= ENSP00000453481.1:n.*589A=
ENST00000560702.1:n.1704A=
ENST00000561208.5:c.1028A= ENSP00000453793.1:p.Asn343=
ENST00000561284.5:n.123A=
ENST00000607277.5:c.605A= ENSP00000475899.1:p.Asn202=
NM_001220482.1:c.1028A= NP_001207411.1:p.Asn343=
NM_002399.3:c.989A= NP_002390.1:p.Asn330=
NM_170674.4:c.1028A= NP_733774.1:p.Asn343=
NM_170675.4:c.1028A= NP_733775.1:p.Asn343=
NM_170676.4:c.1028A= NP_733776.1:p.Asn343=
NM_170677.4:c.1028A= NP_733777.1:p.Asn343=
NM_172315.2:c.989A= NP_758526.1:p.Asn330=
NM_172316.2:c.764A= NP_758527.1:p.Asn255=
NR_051953.1:n.1625A=
XM_006720522.2:c.1028A= XP_006720585.1:p.Asn343=
XM_006720523.1:c.1025A= XP_006720586.1:p.Asn342=
XM_006720524.1:c.1025A= XP_006720587.1:p.Asn342=
XM_006720525.1:c.1025A= XP_006720588.1:p.Asn342=
XM_006720526.2:c.764A= XP_006720589.1:p.Asn255=
XM_006720527.2:c.590A= XP_006720590.1:p.Asn197=
XM_006720528.2:c.590A= XP_006720591.1:p.Asn197=
XM_006720529.2:c.590A= XP_006720592.1:p.Asn197=
XM_011521591.1:c.590A= XP_011519893.1:p.Asn197=
XM_006720526.3:c.764A= XP_006720589.1:p.Asn255=
XM_006720527.3:c.590A= XP_006720590.1:p.Asn197=
XM_006720529.3:c.590A= XP_006720592.1:p.Asn197=
XM_011521591.2:c.590A= XP_011519893.1:p.Asn197=
XM_017022205.2:c.764A= XP_016877694.1:p.Asn255=
XM_024449925.1:c.989A= XP_024305693.1:p.Asn330=
XM_024449926.1:c.989A= XP_024305694.1:p.Asn330=
XM_024449927.1:c.989A= XP_024305695.1:p.Asn330=
XM_024449928.1:c.764A= XP_024305696.1:p.Asn255=
XM_024449929.1:c.989A= XP_024305697.1:p.Asn330=
XR_001751290.2:n.1386A=
XR_002957640.1:n.1339A=
XR_002957641.1:n.1339A=
NM_170675.5:c.1028A= MANE Select NP_733775.1:p.Asn343=
NM_001220482.2:c.1028A= NP_001207411.1:p.Asn343=
NM_170674.5:c.1028A= NP_733774.1:p.Asn343=
NM_170676.5:c.1028A= NP_733776.1:p.Asn343=
NM_170677.5:c.1028A= NP_733777.1:p.Asn343=
NM_172315.3:c.989A= NP_758526.1:p.Asn330=
NR_051953.2:n.2034A=
NM_002399.4:c.989A= NP_002390.1:p.Asn330=
NM_172316.3:c.764A= NP_758527.1:p.Asn255=