Canonical Allele Identifier: CA2580089293

Gene: MEIS2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.37036934_37036938del , CM000677.2:g.37036934_37036938del	GRCh38
NC_000015.9:g.37329135_37329139del , CM000677.1:g.37329135_37329139del	GRCh37
NC_000015.8:g.35116427_35116431del	NCBI36
NG_029108.1:g.69363_69367del

Transcript Alleles

HGVS	Amino-acid Change
NM_170675.5:c.777_781del MANE Select	NP_733775.1:p.Ala260ThrfsTer5
ENST00000561208.6:c.777_781del MANE Select	ENSP00000453793.1:p.Ala260ThrfsTer5
NM_001220482.1:c.777_781del	NP_001207411.1:p.Ala260ThrfsTer5
NM_001220482.2:c.777_781del	NP_001207411.1:p.Ala260ThrfsTer5
NM_002399.3:c.738_742del	NP_002390.1:p.Ala247ThrfsTer5
NM_002399.4:c.738_742del	NP_002390.1:p.Ala247ThrfsTer5
NM_170674.4:c.777_781del	NP_733774.1:p.Ala260ThrfsTer5
NM_170674.5:c.777_781del	NP_733774.1:p.Ala260ThrfsTer5
NM_170675.4:c.777_781del	NP_733775.1:p.Ala260ThrfsTer5
NM_170676.4:c.777_781del	NP_733776.1:p.Ala260ThrfsTer5
NM_170676.5:c.777_781del	NP_733776.1:p.Ala260ThrfsTer5
NM_170677.4:c.777_781del	NP_733777.1:p.Ala260ThrfsTer5
NM_170677.5:c.777_781del	NP_733777.1:p.Ala260ThrfsTer5
NM_172315.2:c.738_742del	NP_758526.1:p.Ala247ThrfsTer5
NM_172315.3:c.738_742del	NP_758526.1:p.Ala247ThrfsTer5
NM_172316.2:c.513_517del	NP_758527.1:p.Ala172ThrfsTer5
NM_172316.3:c.513_517del	NP_758527.1:p.Ala172ThrfsTer5
NR_051953.1:n.1451_1455del
NR_051953.2:n.1860_1864del
ENST00000314177.12:c.777_781del	ENSP00000326296.8:p.Ala260ThrfsTer5
ENST00000338564.9:c.777_781del	ENSP00000341400.4:p.Ala260ThrfsTer5
ENST00000340545.9:c.738_742del	ENSP00000339549.5:p.Ala247ThrfsTer5
ENST00000397620.6:c.513_517del	ENSP00000380745.2:p.Ala172ThrfsTer5
ENST00000397624.7:c.513_517del	ENSP00000380749.3:p.Ala172ThrfsTer5
ENST00000424352.6:c.777_781del	ENSP00000404185.2:p.Ala260ThrfsTer5
ENST00000557796.6:c.738_742del	ENSP00000452693.2:p.Ala247ThrfsTer5
ENST00000559085.5:c.738_742del	ENSP00000453390.1:p.Ala247ThrfsTer5
ENST00000559561.5:c.777_781del	ENSP00000453497.1:p.Ala260ThrfsTer5
ENST00000560570.5:c.*338_*342del	ENSP00000453481.1:n.*338_*342del
ENST00000561163.5:n.1097_1101del
ENST00000561208.5:c.777_781del	ENSP00000453793.1:p.Ala260ThrfsTer5
ENST00000607277.5:c.354_358del	ENSP00000475899.1:p.Ala119ThrfsTer5
ENST00000699901.1:n.100_104del
ENST00000699903.1:c.738_742del	ENSP00000514679.1:p.Ala247ThrfsTer5
ENST00000699904.1:c.738_742del	ENSP00000514680.1:p.Ala247ThrfsTer5
ENST00000699905.1:n.451_455del
ENST00000699955.1:c.777_781del	ENSP00000514715.1:p.Ala260ThrfsTer5
ENST00000699956.1:c.339_343del	ENSP00000514716.1:p.Ala114ThrfsTer5
ENST00000699957.1:n.437_441del
XM_006720522.2:c.777_781del	XP_006720585.1:p.Ala260ThrfsTer5
XM_006720523.1:c.774_778del	XP_006720586.1:p.Ala259ThrfsTer5
XM_006720524.1:c.774_778del	XP_006720587.1:p.Ala259ThrfsTer5
XM_006720525.1:c.774_778del	XP_006720588.1:p.Ala259ThrfsTer5
XM_006720526.2:c.513_517del	XP_006720589.1:p.Ala172ThrfsTer5
XM_006720526.3:c.513_517del	XP_006720589.1:p.Ala172ThrfsTer5
XM_006720527.2:c.339_343del	XP_006720590.1:p.Ala114ThrfsTer5
XM_006720527.3:c.339_343del	XP_006720590.1:p.Ala114ThrfsTer5
XM_006720528.2:c.339_343del	XP_006720591.1:p.Ala114ThrfsTer5
XM_006720529.2:c.339_343del	XP_006720592.1:p.Ala114ThrfsTer5
XM_006720529.3:c.339_343del	XP_006720592.1:p.Ala114ThrfsTer5
XM_011521591.1:c.339_343del	XP_011519893.1:p.Ala114ThrfsTer5
XM_011521591.2:c.339_343del	XP_011519893.1:p.Ala114ThrfsTer5
XM_017022205.2:c.513_517del	XP_016877694.1:p.Ala172ThrfsTer5
XM_024449925.1:c.738_742del	XP_024305693.1:p.Ala247ThrfsTer5
XM_024449926.1:c.738_742del	XP_024305694.1:p.Ala247ThrfsTer5
XM_024449927.1:c.738_742del	XP_024305695.1:p.Ala247ThrfsTer5
XM_024449928.1:c.513_517del	XP_024305696.1:p.Ala172ThrfsTer5
XM_024449929.1:c.738_742del	XP_024305697.1:p.Ala247ThrfsTer5
XR_001751290.2:n.1212_1216del
XR_002957640.1:n.1165_1169del
XR_002957641.1:n.1165_1169del