Canonical Allele Identifier: CA15839444

Gene: MEIS2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.37072053G>A , CM000677.2:g.37072053G>A	GRCh38
NC_000015.9:g.37364254G>A , CM000677.1:g.37364254G>A	GRCh37
NC_000015.8:g.35151546G>A	NCBI36
NG_029108.1:g.34247C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699903.1:c.715+11718C>T	ENSP00000514679.1:n.715+11718C>T
ENST00000699904.1:c.715+11718C>T	ENSP00000514680.1:n.715+11718C>T
ENST00000699905.1:n.428+11718C>T
ENST00000699955.1:c.754+11718C>T	ENSP00000514715.1:n.754+11718C>T
ENST00000699956.1:c.316+11718C>T	ENSP00000514716.1:n.316+11718C>T
ENST00000699957.1:n.414+11718C>T
ENST00000561208.6:c.754+11718C>T MANE Select	ENSP00000453793.1:n.754+11718C>T
ENST00000314177.12:c.754+11718C>T	ENSP00000326296.8:n.754+11718C>T
ENST00000338564.9:c.754+11718C>T	ENSP00000341400.4:n.754+11718C>T
ENST00000340545.9:c.715+11718C>T	ENSP00000339549.5:n.715+11718C>T
ENST00000397620.6:c.490+11718C>T	ENSP00000380745.2:n.490+11718C>T
ENST00000397624.7:c.490+11718C>T	ENSP00000380749.3:n.490+11718C>T
ENST00000424352.6:c.754+11718C>T	ENSP00000404185.2:n.754+11718C>T
ENST00000557796.6:c.715+11718C>T	ENSP00000452693.2:n.715+11718C>T
ENST00000559085.5:c.715+11718C>T	ENSP00000453390.1:n.715+11718C>T
ENST00000559561.5:c.754+11718C>T	ENSP00000453497.1:n.754+11718C>T
ENST00000560570.5:c.*315+11718C>T	ENSP00000453481.1:n.*315+11718C>T
ENST00000561163.5:n.1074+11718C>T
ENST00000561208.5:c.754+11718C>T	ENSP00000453793.1:n.754+11718C>T
ENST00000606653.5:c.305-5516C>T	ENSP00000475660.1:n.305-5516C>T
ENST00000607277.5:c.331+11718C>T	ENSP00000475899.1:n.331+11718C>T
NM_001220482.1:c.754+11718C>T	NP_001207411.1:n.754+11718C>T
NM_002399.3:c.715+11718C>T	NP_002390.1:n.715+11718C>T
NM_170674.4:c.754+11718C>T	NP_733774.1:n.754+11718C>T
NM_170675.4:c.754+11718C>T	NP_733775.1:n.754+11718C>T
NM_170676.4:c.754+11718C>T	NP_733776.1:n.754+11718C>T
NM_170677.4:c.754+11718C>T	NP_733777.1:n.754+11718C>T
NM_172315.2:c.715+11718C>T	NP_758526.1:n.715+11718C>T
NM_172316.2:c.490+11718C>T	NP_758527.1:n.490+11718C>T
NR_051953.1:n.1428+11718C>T
XM_006720522.2:c.754+11718C>T	XP_006720585.1:n.754+11718C>T
XM_006720523.1:c.751+11718C>T	XP_006720586.1:n.751+11718C>T
XM_006720524.1:c.751+11718C>T	XP_006720587.1:n.751+11718C>T
XM_006720525.1:c.751+11718C>T	XP_006720588.1:n.751+11718C>T
XM_006720526.2:c.490+11718C>T	XP_006720589.1:n.490+11718C>T
XM_006720527.2:c.316+11718C>T	XP_006720590.1:n.316+11718C>T
XM_006720528.2:c.316+11718C>T	XP_006720591.1:n.316+11718C>T
XM_006720529.2:c.316+11718C>T	XP_006720592.1:n.316+11718C>T
XM_011521591.1:c.316+11718C>T	XP_011519893.1:n.316+11718C>T
XM_006720526.3:c.490+11718C>T	XP_006720589.1:n.490+11718C>T
XM_006720527.3:c.316+11718C>T	XP_006720590.1:n.316+11718C>T
XM_006720529.3:c.316+11718C>T	XP_006720592.1:n.316+11718C>T
XM_011521591.2:c.316+11718C>T	XP_011519893.1:n.316+11718C>T
XM_017022205.2:c.490+11718C>T	XP_016877694.1:n.490+11718C>T
XM_024449925.1:c.715+11718C>T	XP_024305693.1:n.715+11718C>T
XM_024449926.1:c.715+11718C>T	XP_024305694.1:n.715+11718C>T
XM_024449927.1:c.715+11718C>T	XP_024305695.1:n.715+11718C>T
XM_024449928.1:c.490+11718C>T	XP_024305696.1:n.490+11718C>T
XM_024449929.1:c.715+11718C>T	XP_024305697.1:n.715+11718C>T
XR_001751290.2:n.1189+11718C>T
XR_002957640.1:n.1142+11718C>T
XR_002957641.1:n.1142+11718C>T
NM_170675.5:c.754+11718C>T MANE Select	NP_733775.1:n.754+11718C>T
NM_001220482.2:c.754+11718C>T	NP_001207411.1:n.754+11718C>T
NM_170674.5:c.754+11718C>T	NP_733774.1:n.754+11718C>T
NM_170676.5:c.754+11718C>T	NP_733776.1:n.754+11718C>T
NM_170677.5:c.754+11718C>T	NP_733777.1:n.754+11718C>T
NM_172315.3:c.715+11718C>T	NP_758526.1:n.715+11718C>T
NR_051953.2:n.1837+11718C>T
NM_002399.4:c.715+11718C>T	NP_002390.1:n.715+11718C>T
NM_172316.3:c.490+11718C>T	NP_758527.1:n.490+11718C>T