Canonical Allele Identifier: CA2170135648

Gene: MEIS2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36896504_36896505delinsTA , CM000677.2:g.36896504_36896505delinsTA	GRCh38
NC_000015.9:g.37188705_37188706delinsTA , CM000677.1:g.37188705_37188706delinsTA	GRCh37
NC_000015.8:g.34975997_34975998delinsTA	NCBI36
NG_029108.1:g.209795_209796delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699898.1:n.219+123_219+124delinsTA
ENST00000699899.1:n.219+123_219+124delinsTA
ENST00000699900.1:n.269+123_269+124delinsTA
ENST00000699901.1:n.359+123_359+124delinsTA
ENST00000699902.1:n.199+123_199+124delinsTA
ENST00000699903.1:c.997+123_997+124delinsTA	ENSP00000514679.1:n.997+123_997+124delinsTA
ENST00000699904.1:c.1138+123_1138+124delinsTA	ENSP00000514680.1:n.1138+123_1138+124delinsTA
ENST00000699905.1:n.710+123_710+124delinsTA
ENST00000699906.1:n.263+123_263+124delinsTA
ENST00000699955.1:c.*247+123_*247+124delinsTA	ENSP00000514715.1:n.*247+123_*247+124delinsTA
ENST00000699956.1:c.598+123_598+124delinsTA	ENSP00000514716.1:n.598+123_598+124delinsTA
ENST00000561208.6:c.1036+123_1036+124delinsTA MANE Select	ENSP00000453793.1:n.1036+123_1036+124delinsTA
ENST00000314177.12:c.*50+123_*50+124delinsTA	ENSP00000326296.8:n.*50+123_*50+124delinsTA
ENST00000338564.9:c.1036+123_1036+124delinsTA	ENSP00000341400.4:n.1036+123_1036+124delinsTA
ENST00000340545.9:c.997+123_997+124delinsTA	ENSP00000339549.5:n.997+123_997+124delinsTA
ENST00000397620.6:c.772+123_772+124delinsTA	ENSP00000380745.2:n.772+123_772+124delinsTA
ENST00000397624.7:c.772+123_772+124delinsTA	ENSP00000380749.3:n.772+123_772+124delinsTA
ENST00000424352.6:c.1036+123_1036+124delinsTA	ENSP00000404185.2:n.1036+123_1036+124delinsTA
ENST00000557796.6:c.997+123_997+124delinsTA	ENSP00000452693.2:n.997+123_997+124delinsTA
ENST00000558643.1:n.523+123_523+124delinsTA
ENST00000559085.5:c.997+123_997+124delinsTA	ENSP00000453390.1:n.997+123_997+124delinsTA
ENST00000559371.5:n.357+215_357+216delinsTA
ENST00000559408.1:n.442+123_442+124delinsTA
ENST00000559561.5:c.1036+123_1036+124delinsTA	ENSP00000453497.1:n.1036+123_1036+124delinsTA
ENST00000560570.5:c.*597+123_*597+124delinsTA	ENSP00000453481.1:n.*597+123_*597+124delinsTA
ENST00000560702.1:n.1716+119_1716+120delinsTA
ENST00000561208.5:c.1036+123_1036+124delinsTA	ENSP00000453793.1:n.1036+123_1036+124delinsTA
ENST00000561284.5:n.131+123_131+124delinsTA
ENST00000607277.5:c.613+123_613+124delinsTA	ENSP00000475899.1:n.613+123_613+124delinsTA
NM_001220482.1:c.1036+123_1036+124delinsTA	NP_001207411.1:n.1036+123_1036+124delinsTA
NM_002399.3:c.997+123_997+124delinsTA	NP_002390.1:n.997+123_997+124delinsTA
NM_170674.4:c.1036+123_1036+124delinsTA	NP_733774.1:n.1036+123_1036+124delinsTA
NM_170675.4:c.1036+123_1036+124delinsTA	NP_733775.1:n.1036+123_1036+124delinsTA
NM_170676.4:c.1036+123_1036+124delinsTA	NP_733776.1:n.1036+123_1036+124delinsTA
NM_170677.4:c.1036+123_1036+124delinsTA	NP_733777.1:n.1036+123_1036+124delinsTA
NM_172315.2:c.997+123_997+124delinsTA	NP_758526.1:n.997+123_997+124delinsTA
NM_172316.2:c.772+123_772+124delinsTA	NP_758527.1:n.772+123_772+124delinsTA
NR_051953.1:n.1633+123_1633+124delinsTA
XM_006720522.2:c.1036+123_1036+124delinsTA	XP_006720585.1:n.1036+123_1036+124delinsTA
XM_006720523.1:c.1033+123_1033+124delinsTA	XP_006720586.1:n.1033+123_1033+124delinsTA
XM_006720524.1:c.1033+123_1033+124delinsTA	XP_006720587.1:n.1033+123_1033+124delinsTA
XM_006720525.1:c.1033+123_1033+124delinsTA	XP_006720588.1:n.1033+123_1033+124delinsTA
XM_006720526.2:c.772+123_772+124delinsTA	XP_006720589.1:n.772+123_772+124delinsTA
XM_006720527.2:c.598+123_598+124delinsTA	XP_006720590.1:n.598+123_598+124delinsTA
XM_006720528.2:c.598+123_598+124delinsTA	XP_006720591.1:n.598+123_598+124delinsTA
XM_006720529.2:c.598+123_598+124delinsTA	XP_006720592.1:n.598+123_598+124delinsTA
XM_011521591.1:c.598+123_598+124delinsTA	XP_011519893.1:n.598+123_598+124delinsTA
XM_006720526.3:c.772+123_772+124delinsTA	XP_006720589.1:n.772+123_772+124delinsTA
XM_006720527.3:c.598+123_598+124delinsTA	XP_006720590.1:n.598+123_598+124delinsTA
XM_006720529.3:c.598+123_598+124delinsTA	XP_006720592.1:n.598+123_598+124delinsTA
XM_011521591.2:c.598+123_598+124delinsTA	XP_011519893.1:n.598+123_598+124delinsTA
XM_017022205.2:c.772+123_772+124delinsTA	XP_016877694.1:n.772+123_772+124delinsTA
XM_024449925.1:c.997+123_997+124delinsTA	XP_024305693.1:n.997+123_997+124delinsTA
XM_024449926.1:c.997+123_997+124delinsTA	XP_024305694.1:n.997+123_997+124delinsTA
XM_024449927.1:c.997+123_997+124delinsTA	XP_024305695.1:n.997+123_997+124delinsTA
XM_024449928.1:c.772+123_772+124delinsTA	XP_024305696.1:n.772+123_772+124delinsTA
XM_024449929.1:c.997+123_997+124delinsTA	XP_024305697.1:n.997+123_997+124delinsTA
XR_001751290.2:n.1394+123_1394+124delinsTA
XR_002957640.1:n.1347+123_1347+124delinsTA
XR_002957641.1:n.1347+123_1347+124delinsTA
NM_170675.5:c.1036+123_1036+124delinsTA MANE Select	NP_733775.1:n.1036+123_1036+124delinsTA
NM_001220482.2:c.1036+123_1036+124delinsTA	NP_001207411.1:n.1036+123_1036+124delinsTA
NM_170674.5:c.1036+123_1036+124delinsTA	NP_733774.1:n.1036+123_1036+124delinsTA
NM_170676.5:c.1036+123_1036+124delinsTA	NP_733776.1:n.1036+123_1036+124delinsTA
NM_170677.5:c.1036+123_1036+124delinsTA	NP_733777.1:n.1036+123_1036+124delinsTA
NM_172315.3:c.997+123_997+124delinsTA	NP_758526.1:n.997+123_997+124delinsTA
NR_051953.2:n.2042+123_2042+124delinsTA
NM_002399.4:c.997+123_997+124delinsTA	NP_002390.1:n.997+123_997+124delinsTA
NM_172316.3:c.772+123_772+124delinsTA	NP_758527.1:n.772+123_772+124delinsTA