Canonical Allele Identifier: CA391927040

Gene: MEIS2

Linked Data

• MyVariant Identifiers: chr15:g.37242538G>T (hg19) ; chr15:g.36950337G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36950337G>T , CM000677.2:g.36950337G>T	GRCh38
NC_000015.9:g.37242538G>T , CM000677.1:g.37242538G>T	GRCh37
NC_000015.8:g.35029830G>T	NCBI36
NG_029108.1:g.155963C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000699898.1:n.147C>A
ENST00000699899.1:n.147C>A
ENST00000699900.1:n.197C>A
ENST00000699901.1:n.287C>A
ENST00000699902.1:n.127C>A
ENST00000699903.1:c.925C>A	ENSP00000514679.1:p.Gln309Lys
ENST00000699904.1:c.925C>A	ENSP00000514680.1:p.Gln309Lys
ENST00000699905.1:n.638C>A
ENST00000699955.1:c.*175C>A	ENSP00000514715.1:n.*175C>A
ENST00000699956.1:c.526C>A	ENSP00000514716.1:p.Gln176Lys
ENST00000561208.6:c.964C>A MANE Select	ENSP00000453793.1:p.Gln322Lys
ENST00000314177.12:c.901-53651C>A	ENSP00000326296.8:n.901-53651C>A
ENST00000338564.9:c.964C>A	ENSP00000341400.4:p.Gln322Lys
ENST00000340545.9:c.925C>A	ENSP00000339549.5:p.Gln309Lys
ENST00000397620.6:c.700C>A	ENSP00000380745.2:p.Gln234Lys
ENST00000397624.7:c.700C>A	ENSP00000380749.3:p.Gln234Lys
ENST00000424352.6:c.964C>A	ENSP00000404185.2:p.Gln322Lys
ENST00000557796.6:c.925C>A	ENSP00000452693.2:p.Gln309Lys
ENST00000559085.5:c.925C>A	ENSP00000453390.1:p.Gln309Lys
ENST00000559561.5:c.964C>A	ENSP00000453497.1:p.Gln322Lys
ENST00000560570.5:c.*525C>A	ENSP00000453481.1:n.*525C>A
ENST00000561208.5:c.964C>A	ENSP00000453793.1:p.Gln322Lys
ENST00000607277.5:c.541C>A	ENSP00000475899.1:p.Gln181Lys
NM_001220482.1:c.964C>A	NP_001207411.1:p.Gln322Lys
NM_002399.3:c.925C>A	NP_002390.1:p.Gln309Lys
NM_170674.4:c.964C>A	NP_733774.1:p.Gln322Lys
NM_170675.4:c.964C>A	NP_733775.1:p.Gln322Lys
NM_170676.4:c.964C>A	NP_733776.1:p.Gln322Lys
NM_170677.4:c.964C>A	NP_733777.1:p.Gln322Lys
NM_172315.2:c.925C>A	NP_758526.1:p.Gln309Lys
NM_172316.2:c.700C>A	NP_758527.1:p.Gln234Lys
NR_051953.1:n.1575-53651C>A
XM_006720522.2:c.964C>A	XP_006720585.1:p.Gln322Lys
XM_006720523.1:c.961C>A	XP_006720586.1:p.Gln321Lys
XM_006720524.1:c.961C>A	XP_006720587.1:p.Gln321Lys
XM_006720525.1:c.961C>A	XP_006720588.1:p.Gln321Lys
XM_006720526.2:c.700C>A	XP_006720589.1:p.Gln234Lys
XM_006720527.2:c.526C>A	XP_006720590.1:p.Gln176Lys
XM_006720528.2:c.526C>A	XP_006720591.1:p.Gln176Lys
XM_006720529.2:c.526C>A	XP_006720592.1:p.Gln176Lys
XM_011521591.1:c.526C>A	XP_011519893.1:p.Gln176Lys
XM_006720526.3:c.700C>A	XP_006720589.1:p.Gln234Lys
XM_006720527.3:c.526C>A	XP_006720590.1:p.Gln176Lys
XM_006720529.3:c.526C>A	XP_006720592.1:p.Gln176Lys
XM_011521591.2:c.526C>A	XP_011519893.1:p.Gln176Lys
XM_017022205.2:c.700C>A	XP_016877694.1:p.Gln234Lys
XM_024449925.1:c.925C>A	XP_024305693.1:p.Gln309Lys
XM_024449926.1:c.925C>A	XP_024305694.1:p.Gln309Lys
XM_024449927.1:c.925C>A	XP_024305695.1:p.Gln309Lys
XM_024449928.1:c.700C>A	XP_024305696.1:p.Gln234Lys
XM_024449929.1:c.925C>A	XP_024305697.1:p.Gln309Lys
XR_001751290.2:n.1336-53651C>A
XR_002957640.1:n.1289-53651C>A
XR_002957641.1:n.1289-53651C>A
NM_170675.5:c.964C>A MANE Select	NP_733775.1:p.Gln322Lys
NM_001220482.2:c.964C>A	NP_001207411.1:p.Gln322Lys
NM_170674.5:c.964C>A	NP_733774.1:p.Gln322Lys
NM_170676.5:c.964C>A	NP_733776.1:p.Gln322Lys
NM_170677.5:c.964C>A	NP_733777.1:p.Gln322Lys
NM_172315.3:c.925C>A	NP_758526.1:p.Gln309Lys
NR_051953.2:n.1984-53651C>A
NM_002399.4:c.925C>A	NP_002390.1:p.Gln309Lys
NM_172316.3:c.700C>A	NP_758527.1:p.Gln234Lys