Canonical Allele Identifier: CA2170135546

Gene: MEIS2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36896353C= , CM000677.2:g.36896353C=	GRCh38
NC_000015.9:g.37188554C= , CM000677.1:g.37188554C=	GRCh37
NC_000015.8:g.34975846C=	NCBI36
NG_029108.1:g.209947G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699898.1:n.219+275G=
ENST00000699899.1:n.219+275G=
ENST00000699900.1:n.269+275G=
ENST00000699901.1:n.359+275G=
ENST00000699902.1:n.199+275G=
ENST00000699903.1:c.997+275G=	ENSP00000514679.1:n.997+275G=
ENST00000699904.1:c.1138+275G=	ENSP00000514680.1:n.1138+275G=
ENST00000699905.1:n.710+275G=
ENST00000699906.1:n.263+275G=
ENST00000699955.1:c.*247+275G=	ENSP00000514715.1:n.*247+275G=
ENST00000699956.1:c.598+275G=	ENSP00000514716.1:n.598+275G=
ENST00000561208.6:c.1036+275G= MANE Select	ENSP00000453793.1:n.1036+275G=
ENST00000314177.12:c.*50+275G=	ENSP00000326296.8:n.*50+275G=
ENST00000338564.9:c.1036+275G=	ENSP00000341400.4:n.1036+275G=
ENST00000340545.9:c.997+275G=	ENSP00000339549.5:n.997+275G=
ENST00000397620.6:c.772+275G=	ENSP00000380745.2:n.772+275G=
ENST00000397624.7:c.772+275G=	ENSP00000380749.3:n.772+275G=
ENST00000424352.6:c.1036+275G=	ENSP00000404185.2:n.1036+275G=
ENST00000557796.6:c.997+275G=	ENSP00000452693.2:n.997+275G=
ENST00000558643.1:n.523+275G=
ENST00000559085.5:c.997+275G=	ENSP00000453390.1:n.997+275G=
ENST00000559371.5:n.357+367G=
ENST00000559408.1:n.442+275G=
ENST00000559561.5:c.1036+275G=	ENSP00000453497.1:n.1036+275G=
ENST00000560570.5:c.*597+275G=	ENSP00000453481.1:n.*597+275G=
ENST00000560702.1:n.1716+271G=
ENST00000561208.5:c.1036+275G=	ENSP00000453793.1:n.1036+275G=
ENST00000561284.5:n.131+275G=
ENST00000607277.5:c.613+275G=	ENSP00000475899.1:n.613+275G=
NM_001220482.1:c.1036+275G=	NP_001207411.1:n.1036+275G=
NM_002399.3:c.997+275G=	NP_002390.1:n.997+275G=
NM_170674.4:c.1036+275G=	NP_733774.1:n.1036+275G=
NM_170675.4:c.1036+275G=	NP_733775.1:n.1036+275G=
NM_170676.4:c.1036+275G=	NP_733776.1:n.1036+275G=
NM_170677.4:c.1036+275G=	NP_733777.1:n.1036+275G=
NM_172315.2:c.997+275G=	NP_758526.1:n.997+275G=
NM_172316.2:c.772+275G=	NP_758527.1:n.772+275G=
NR_051953.1:n.1633+275G=
XM_006720522.2:c.1036+275G=	XP_006720585.1:n.1036+275G=
XM_006720523.1:c.1033+275G=	XP_006720586.1:n.1033+275G=
XM_006720524.1:c.1033+275G=	XP_006720587.1:n.1033+275G=
XM_006720525.1:c.1033+275G=	XP_006720588.1:n.1033+275G=
XM_006720526.2:c.772+275G=	XP_006720589.1:n.772+275G=
XM_006720527.2:c.598+275G=	XP_006720590.1:n.598+275G=
XM_006720528.2:c.598+275G=	XP_006720591.1:n.598+275G=
XM_006720529.2:c.598+275G=	XP_006720592.1:n.598+275G=
XM_011521591.1:c.598+275G=	XP_011519893.1:n.598+275G=
XM_006720526.3:c.772+275G=	XP_006720589.1:n.772+275G=
XM_006720527.3:c.598+275G=	XP_006720590.1:n.598+275G=
XM_006720529.3:c.598+275G=	XP_006720592.1:n.598+275G=
XM_011521591.2:c.598+275G=	XP_011519893.1:n.598+275G=
XM_017022205.2:c.772+275G=	XP_016877694.1:n.772+275G=
XM_024449925.1:c.997+275G=	XP_024305693.1:n.997+275G=
XM_024449926.1:c.997+275G=	XP_024305694.1:n.997+275G=
XM_024449927.1:c.997+275G=	XP_024305695.1:n.997+275G=
XM_024449928.1:c.772+275G=	XP_024305696.1:n.772+275G=
XM_024449929.1:c.997+275G=	XP_024305697.1:n.997+275G=
XR_001751290.2:n.1394+275G=
XR_002957640.1:n.1347+275G=
XR_002957641.1:n.1347+275G=
NM_170675.5:c.1036+275G= MANE Select	NP_733775.1:n.1036+275G=
NM_001220482.2:c.1036+275G=	NP_001207411.1:n.1036+275G=
NM_170674.5:c.1036+275G=	NP_733774.1:n.1036+275G=
NM_170676.5:c.1036+275G=	NP_733776.1:n.1036+275G=
NM_170677.5:c.1036+275G=	NP_733777.1:n.1036+275G=
NM_172315.3:c.997+275G=	NP_758526.1:n.997+275G=
NR_051953.2:n.2042+275G=
NM_002399.4:c.997+275G=	NP_002390.1:n.997+275G=
NM_172316.3:c.772+275G=	NP_758527.1:n.772+275G=