Canonical Allele Identifier: CA7469187

Gene: MEIS2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36895134G>A , CM000677.2:g.36895134G>A	GRCh38
NC_000015.9:g.37187335G>A , CM000677.1:g.37187335G>A	GRCh37
NC_000015.8:g.34974627G>A	NCBI36
NG_029108.1:g.211166C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699898.1:n.330+17C>T
ENST00000699899.1:n.330+17C>T
ENST00000699900.1:n.380+17C>T
ENST00000699901.1:n.470+17C>T
ENST00000699902.1:n.310+17C>T
ENST00000699903.1:c.1087+17C>T	ENSP00000514679.1:n.1087+17C>T
ENST00000699904.1:c.1249+17C>T	ENSP00000514680.1:n.1249+17C>T
ENST00000699905.1:n.800+17C>T
ENST00000699906.1:n.374+17C>T
ENST00000699955.1:c.*358+17C>T	ENSP00000514715.1:n.*358+17C>T
ENST00000699956.1:c.688+17C>T	ENSP00000514716.1:n.688+17C>T
ENST00000561208.6:c.1147+17C>T MANE Select	ENSP00000453793.1:n.1147+17C>T
ENST00000314177.12:c.*140+17C>T	ENSP00000326296.8:n.*140+17C>T
ENST00000338564.9:c.1126+17C>T	ENSP00000341400.4:n.1126+17C>T
ENST00000340545.9:c.1087+17C>T	ENSP00000339549.5:n.1087+17C>T
ENST00000397620.6:c.862+17C>T	ENSP00000380745.2:n.862+17C>T
ENST00000397624.7:c.862+17C>T	ENSP00000380749.3:n.862+17C>T
ENST00000424352.6:c.1147+17C>T	ENSP00000404185.2:n.1147+17C>T
ENST00000557796.6:c.1087+17C>T	ENSP00000452693.2:n.1087+17C>T
ENST00000557992.1:n.152+17C>T
ENST00000558643.1:n.634+17C>T
ENST00000559085.5:c.1108+17C>T	ENSP00000453390.1:n.1108+17C>T
ENST00000559371.5:n.447+17C>T
ENST00000559408.1:n.532+17C>T
ENST00000559561.5:c.1126+17C>T	ENSP00000453497.1:n.1126+17C>T
ENST00000559972.1:n.137+17C>T
ENST00000560570.5:c.*708+17C>T	ENSP00000453481.1:n.*708+17C>T
ENST00000560702.1:n.1802+17C>T
ENST00000561208.5:c.1147+17C>T	ENSP00000453793.1:n.1147+17C>T
ENST00000561264.6:n.128+17C>T
ENST00000561284.5:n.221+17C>T
NM_001220482.1:c.1126+17C>T	NP_001207411.1:n.1126+17C>T
NM_002399.3:c.1087+17C>T	NP_002390.1:n.1087+17C>T
NM_170674.4:c.1126+17C>T	NP_733774.1:n.1126+17C>T
NM_170675.4:c.1147+17C>T	NP_733775.1:n.1147+17C>T
NM_170676.4:c.1126+17C>T	NP_733776.1:n.1126+17C>T
NM_170677.4:c.1147+17C>T	NP_733777.1:n.1147+17C>T
NM_172315.2:c.1108+17C>T	NP_758526.1:n.1108+17C>T
NM_172316.2:c.862+17C>T	NP_758527.1:n.862+17C>T
NR_051953.1:n.1723+17C>T
XM_006720522.2:c.1147+17C>T	XP_006720585.1:n.1147+17C>T
XM_006720523.1:c.1144+17C>T	XP_006720586.1:n.1144+17C>T
XM_006720524.1:c.1144+17C>T	XP_006720587.1:n.1144+17C>T
XM_006720525.1:c.1123+17C>T	XP_006720588.1:n.1123+17C>T
XM_006720526.2:c.883+17C>T	XP_006720589.1:n.883+17C>T
XM_006720527.2:c.709+17C>T	XP_006720590.1:n.709+17C>T
XM_006720528.2:c.709+17C>T	XP_006720591.1:n.709+17C>T
XM_006720529.2:c.709+17C>T	XP_006720592.1:n.709+17C>T
XM_011521591.1:c.709+17C>T	XP_011519893.1:n.709+17C>T
XM_006720526.3:c.883+17C>T	XP_006720589.1:n.883+17C>T
XM_006720527.3:c.709+17C>T	XP_006720590.1:n.709+17C>T
XM_006720529.3:c.709+17C>T	XP_006720592.1:n.709+17C>T
XM_011521591.2:c.709+17C>T	XP_011519893.1:n.709+17C>T
XM_017022205.2:c.862+17C>T	XP_016877694.1:n.862+17C>T
XM_024449925.1:c.1108+17C>T	XP_024305693.1:n.1108+17C>T
XM_024449926.1:c.1108+17C>T	XP_024305694.1:n.1108+17C>T
XM_024449927.1:c.1087+17C>T	XP_024305695.1:n.1087+17C>T
XM_024449928.1:c.883+17C>T	XP_024305696.1:n.883+17C>T
XM_024449929.1:c.1108+17C>T	XP_024305697.1:n.1108+17C>T
XR_001751290.2:n.1505+17C>T
XR_002957640.1:n.1458+17C>T
XR_002957641.1:n.1437+17C>T
NM_170675.5:c.1147+17C>T MANE Select	NP_733775.1:n.1147+17C>T
NM_001220482.2:c.1126+17C>T	NP_001207411.1:n.1126+17C>T
NM_170674.5:c.1126+17C>T	NP_733774.1:n.1126+17C>T
NM_170676.5:c.1126+17C>T	NP_733776.1:n.1126+17C>T
NM_170677.5:c.1147+17C>T	NP_733777.1:n.1147+17C>T
NM_172315.3:c.1108+17C>T	NP_758526.1:n.1108+17C>T
NR_051953.2:n.2132+17C>T
NM_002399.4:c.1087+17C>T	NP_002390.1:n.1087+17C>T
NM_172316.3:c.862+17C>T	NP_758527.1:n.862+17C>T