Canonical Allele Identifier: CA391926957

Gene: MEIS2

Linked Data

• MyVariant Identifiers: chr15:g.37188873C>A (hg19) ; chr15:g.36896672C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36896672C>A , CM000677.2:g.36896672C>A	GRCh38
NC_000015.9:g.37188873C>A , CM000677.1:g.37188873C>A	GRCh37
NC_000015.8:g.34976165C>A	NCBI36
NG_029108.1:g.209628G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699898.1:n.175G>T
ENST00000699899.1:n.175G>T
ENST00000699900.1:n.225G>T
ENST00000699901.1:n.315G>T
ENST00000699902.1:n.155G>T
ENST00000699903.1:c.953G>T	ENSP00000514679.1:p.Arg318Ile
ENST00000699904.1:c.1094G>T	ENSP00000514680.1:p.Arg365Ile
ENST00000699905.1:n.666G>T
ENST00000699906.1:n.219G>T
ENST00000699955.1:c.*203G>T	ENSP00000514715.1:n.*203G>T
ENST00000699956.1:c.554G>T	ENSP00000514716.1:p.Arg185Ile
ENST00000561208.6:c.992G>T MANE Select	ENSP00000453793.1:p.Arg331Ile
ENST00000314177.12:c.*6G>T	ENSP00000326296.8:n.*6G>T
ENST00000338564.9:c.992G>T	ENSP00000341400.4:p.Arg331Ile
ENST00000340545.9:c.953G>T	ENSP00000339549.5:p.Arg318Ile
ENST00000397620.6:c.728G>T	ENSP00000380745.2:p.Arg243Ile
ENST00000397624.7:c.728G>T	ENSP00000380749.3:p.Arg243Ile
ENST00000424352.6:c.992G>T	ENSP00000404185.2:p.Arg331Ile
ENST00000557796.6:c.953G>T	ENSP00000452693.2:p.Arg318Ile
ENST00000558643.1:n.479G>T
ENST00000559085.5:c.953G>T	ENSP00000453390.1:p.Arg318Ile
ENST00000559371.5:n.357+48G>T
ENST00000559408.1:n.398G>T
ENST00000559561.5:c.992G>T	ENSP00000453497.1:p.Arg331Ile
ENST00000560570.5:c.*553G>T	ENSP00000453481.1:n.*553G>T
ENST00000560702.1:n.1668G>T
ENST00000561208.5:c.992G>T	ENSP00000453793.1:p.Arg331Ile
ENST00000561284.5:n.87G>T
ENST00000607277.5:c.569G>T	ENSP00000475899.1:p.Arg190Ile
NM_001220482.1:c.992G>T	NP_001207411.1:p.Arg331Ile
NM_002399.3:c.953G>T	NP_002390.1:p.Arg318Ile
NM_170674.4:c.992G>T	NP_733774.1:p.Arg331Ile
NM_170675.4:c.992G>T	NP_733775.1:p.Arg331Ile
NM_170676.4:c.992G>T	NP_733776.1:p.Arg331Ile
NM_170677.4:c.992G>T	NP_733777.1:p.Arg331Ile
NM_172315.2:c.953G>T	NP_758526.1:p.Arg318Ile
NM_172316.2:c.728G>T	NP_758527.1:p.Arg243Ile
NR_051953.1:n.1589G>T
XM_006720522.2:c.992G>T	XP_006720585.1:p.Arg331Ile
XM_006720523.1:c.989G>T	XP_006720586.1:p.Arg330Ile
XM_006720524.1:c.989G>T	XP_006720587.1:p.Arg330Ile
XM_006720525.1:c.989G>T	XP_006720588.1:p.Arg330Ile
XM_006720526.2:c.728G>T	XP_006720589.1:p.Arg243Ile
XM_006720527.2:c.554G>T	XP_006720590.1:p.Arg185Ile
XM_006720528.2:c.554G>T	XP_006720591.1:p.Arg185Ile
XM_006720529.2:c.554G>T	XP_006720592.1:p.Arg185Ile
XM_011521591.1:c.554G>T	XP_011519893.1:p.Arg185Ile
XM_006720526.3:c.728G>T	XP_006720589.1:p.Arg243Ile
XM_006720527.3:c.554G>T	XP_006720590.1:p.Arg185Ile
XM_006720529.3:c.554G>T	XP_006720592.1:p.Arg185Ile
XM_011521591.2:c.554G>T	XP_011519893.1:p.Arg185Ile
XM_017022205.2:c.728G>T	XP_016877694.1:p.Arg243Ile
XM_024449925.1:c.953G>T	XP_024305693.1:p.Arg318Ile
XM_024449926.1:c.953G>T	XP_024305694.1:p.Arg318Ile
XM_024449927.1:c.953G>T	XP_024305695.1:p.Arg318Ile
XM_024449928.1:c.728G>T	XP_024305696.1:p.Arg243Ile
XM_024449929.1:c.953G>T	XP_024305697.1:p.Arg318Ile
XR_001751290.2:n.1350G>T
XR_002957640.1:n.1303G>T
XR_002957641.1:n.1303G>T
NM_170675.5:c.992G>T MANE Select	NP_733775.1:p.Arg331Ile
NM_001220482.2:c.992G>T	NP_001207411.1:p.Arg331Ile
NM_170674.5:c.992G>T	NP_733774.1:p.Arg331Ile
NM_170676.5:c.992G>T	NP_733776.1:p.Arg331Ile
NM_170677.5:c.992G>T	NP_733777.1:p.Arg331Ile
NM_172315.3:c.953G>T	NP_758526.1:p.Arg318Ile
NR_051953.2:n.1998G>T
NM_002399.4:c.953G>T	NP_002390.1:p.Arg318Ile
NM_172316.3:c.728G>T	NP_758527.1:p.Arg243Ile