Canonical Allele Identifier: CA2170159656
Community Standard Title: NM_170675.5(MEIS2):c.905C= (p.Pro302=)
Gene: MEIS2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_170675.5:c.905C= MANE Select NP_733775.1:p.Pro302=
ENST00000561208.6:c.905C= MANE Select ENSP00000453793.1:p.Pro302=
NM_001220482.1:c.905C= NP_001207411.1:p.Pro302=
NM_001220482.2:c.905C= NP_001207411.1:p.Pro302=
NM_002399.3:c.866C= NP_002390.1:p.Pro289=
NM_002399.4:c.866C= NP_002390.1:p.Pro289=
NM_170674.4:c.905C= NP_733774.1:p.Pro302=
NM_170674.5:c.905C= NP_733774.1:p.Pro302=
NM_170675.4:c.905C= NP_733775.1:p.Pro302=
NM_170676.4:c.905C= NP_733776.1:p.Pro302=
NM_170676.5:c.905C= NP_733776.1:p.Pro302=
NM_170677.4:c.905C= NP_733777.1:p.Pro302=
NM_170677.5:c.905C= NP_733777.1:p.Pro302=
NM_172315.2:c.866C= NP_758526.1:p.Pro289=
NM_172315.3:c.866C= NP_758526.1:p.Pro289=
NM_172316.2:c.641C= NP_758527.1:p.Pro214=
NM_172316.3:c.641C= NP_758527.1:p.Pro214=
NR_051953.1:n.1575-53710C=
NR_051953.2:n.1984-53710C=
ENST00000314177.12:c.901-53710C= ENSP00000326296.8:n.901-53710C=
ENST00000338564.9:c.905C= ENSP00000341400.4:p.Pro302=
ENST00000340545.9:c.866C= ENSP00000339549.5:p.Pro289=
ENST00000397620.6:c.641C= ENSP00000380745.2:p.Pro214=
ENST00000397624.7:c.641C= ENSP00000380749.3:p.Pro214=
ENST00000424352.6:c.905C= ENSP00000404185.2:p.Pro302=
ENST00000557796.6:c.866C= ENSP00000452693.2:p.Pro289=
ENST00000559085.5:c.866C= ENSP00000453390.1:p.Pro289=
ENST00000559561.5:c.905C= ENSP00000453497.1:p.Pro302=
ENST00000560570.5:c.*466C= ENSP00000453481.1:n.*466C=
ENST00000561208.5:c.905C= ENSP00000453793.1:p.Pro302=
ENST00000607277.5:c.482C= ENSP00000475899.1:p.Pro161=
ENST00000699898.1:n.88C=
ENST00000699899.1:n.88C=
ENST00000699900.1:n.138C=
ENST00000699901.1:n.228C=
ENST00000699902.1:n.68C=
ENST00000699903.1:c.866C= ENSP00000514679.1:p.Pro289=
ENST00000699904.1:c.866C= ENSP00000514680.1:p.Pro289=
ENST00000699905.1:n.579C=
ENST00000699955.1:c.*116C= ENSP00000514715.1:n.*116C=
ENST00000699956.1:c.467C= ENSP00000514716.1:p.Pro156=
XM_006720522.2:c.905C= XP_006720585.1:p.Pro302=
XM_006720523.1:c.902C= XP_006720586.1:p.Pro301=
XM_006720524.1:c.902C= XP_006720587.1:p.Pro301=
XM_006720525.1:c.902C= XP_006720588.1:p.Pro301=
XM_006720526.2:c.641C= XP_006720589.1:p.Pro214=
XM_006720526.3:c.641C= XP_006720589.1:p.Pro214=
XM_006720527.2:c.467C= XP_006720590.1:p.Pro156=
XM_006720527.3:c.467C= XP_006720590.1:p.Pro156=
XM_006720528.2:c.467C= XP_006720591.1:p.Pro156=
XM_006720529.2:c.467C= XP_006720592.1:p.Pro156=
XM_006720529.3:c.467C= XP_006720592.1:p.Pro156=
XM_011521591.1:c.467C= XP_011519893.1:p.Pro156=
XM_011521591.2:c.467C= XP_011519893.1:p.Pro156=
XM_017022205.2:c.641C= XP_016877694.1:p.Pro214=
XM_024449925.1:c.866C= XP_024305693.1:p.Pro289=
XM_024449926.1:c.866C= XP_024305694.1:p.Pro289=
XM_024449927.1:c.866C= XP_024305695.1:p.Pro289=
XM_024449928.1:c.641C= XP_024305696.1:p.Pro214=
XM_024449929.1:c.866C= XP_024305697.1:p.Pro289=
XR_001751290.2:n.1336-53710C=
XR_002957640.1:n.1289-53710C=
XR_002957641.1:n.1289-53710C=