Canonical Allele Identifier: CA391926865

Gene: MEIS2

Linked Data

• ClinVar Variation Id: 1432617
• ClinVar RCV Id: RCV001943992
• dbSNP Id: rs2141225052
• gnomAD v4: 15-36896633-C-T
• MyVariant Identifiers: chr15:g.37188834C>T (hg19) ; chr15:g.36896633C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36896633C>T , CM000677.2:g.36896633C>T	GRCh38
NC_000015.9:g.37188834C>T , CM000677.1:g.37188834C>T	GRCh37
NC_000015.8:g.34976126C>T	NCBI36
NG_029108.1:g.209667G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699898.1:n.214G>A
ENST00000699899.1:n.214G>A
ENST00000699900.1:n.264G>A
ENST00000699901.1:n.354G>A
ENST00000699902.1:n.194G>A
ENST00000699903.1:c.992G>A	ENSP00000514679.1:p.Arg331Gln
ENST00000699904.1:c.1133G>A	ENSP00000514680.1:p.Arg378Gln
ENST00000699905.1:n.705G>A
ENST00000699906.1:n.258G>A
ENST00000699955.1:c.*242G>A	ENSP00000514715.1:n.*242G>A
ENST00000699956.1:c.593G>A	ENSP00000514716.1:p.Arg198Gln
ENST00000561208.6:c.1031G>A MANE Select	ENSP00000453793.1:p.Arg344Gln
ENST00000314177.12:c.*45G>A	ENSP00000326296.8:n.*45G>A
ENST00000338564.9:c.1031G>A	ENSP00000341400.4:p.Arg344Gln
ENST00000340545.9:c.992G>A	ENSP00000339549.5:p.Arg331Gln
ENST00000397620.6:c.767G>A	ENSP00000380745.2:p.Arg256Gln
ENST00000397624.7:c.767G>A	ENSP00000380749.3:p.Arg256Gln
ENST00000424352.6:c.1031G>A	ENSP00000404185.2:p.Arg344Gln
ENST00000557796.6:c.992G>A	ENSP00000452693.2:p.Arg331Gln
ENST00000558643.1:n.518G>A
ENST00000559085.5:c.992G>A	ENSP00000453390.1:p.Arg331Gln
ENST00000559371.5:n.357+87G>A
ENST00000559408.1:n.437G>A
ENST00000559561.5:c.1031G>A	ENSP00000453497.1:p.Arg344Gln
ENST00000560570.5:c.*592G>A	ENSP00000453481.1:n.*592G>A
ENST00000560702.1:n.1707G>A
ENST00000561208.5:c.1031G>A	ENSP00000453793.1:p.Arg344Gln
ENST00000561284.5:n.126G>A
ENST00000607277.5:c.608G>A	ENSP00000475899.1:p.Arg203Gln
NM_001220482.1:c.1031G>A	NP_001207411.1:p.Arg344Gln
NM_002399.3:c.992G>A	NP_002390.1:p.Arg331Gln
NM_170674.4:c.1031G>A	NP_733774.1:p.Arg344Gln
NM_170675.4:c.1031G>A	NP_733775.1:p.Arg344Gln
NM_170676.4:c.1031G>A	NP_733776.1:p.Arg344Gln
NM_170677.4:c.1031G>A	NP_733777.1:p.Arg344Gln
NM_172315.2:c.992G>A	NP_758526.1:p.Arg331Gln
NM_172316.2:c.767G>A	NP_758527.1:p.Arg256Gln
NR_051953.1:n.1628G>A
XM_006720522.2:c.1031G>A	XP_006720585.1:p.Arg344Gln
XM_006720523.1:c.1028G>A	XP_006720586.1:p.Arg343Gln
XM_006720524.1:c.1028G>A	XP_006720587.1:p.Arg343Gln
XM_006720525.1:c.1028G>A	XP_006720588.1:p.Arg343Gln
XM_006720526.2:c.767G>A	XP_006720589.1:p.Arg256Gln
XM_006720527.2:c.593G>A	XP_006720590.1:p.Arg198Gln
XM_006720528.2:c.593G>A	XP_006720591.1:p.Arg198Gln
XM_006720529.2:c.593G>A	XP_006720592.1:p.Arg198Gln
XM_011521591.1:c.593G>A	XP_011519893.1:p.Arg198Gln
XM_006720526.3:c.767G>A	XP_006720589.1:p.Arg256Gln
XM_006720527.3:c.593G>A	XP_006720590.1:p.Arg198Gln
XM_006720529.3:c.593G>A	XP_006720592.1:p.Arg198Gln
XM_011521591.2:c.593G>A	XP_011519893.1:p.Arg198Gln
XM_017022205.2:c.767G>A	XP_016877694.1:p.Arg256Gln
XM_024449925.1:c.992G>A	XP_024305693.1:p.Arg331Gln
XM_024449926.1:c.992G>A	XP_024305694.1:p.Arg331Gln
XM_024449927.1:c.992G>A	XP_024305695.1:p.Arg331Gln
XM_024449928.1:c.767G>A	XP_024305696.1:p.Arg256Gln
XM_024449929.1:c.992G>A	XP_024305697.1:p.Arg331Gln
XR_001751290.2:n.1389G>A
XR_002957640.1:n.1342G>A
XR_002957641.1:n.1342G>A
NM_170675.5:c.1031G>A MANE Select	NP_733775.1:p.Arg344Gln
NM_001220482.2:c.1031G>A	NP_001207411.1:p.Arg344Gln
NM_170674.5:c.1031G>A	NP_733774.1:p.Arg344Gln
NM_170676.5:c.1031G>A	NP_733776.1:p.Arg344Gln
NM_170677.5:c.1031G>A	NP_733777.1:p.Arg344Gln
NM_172315.3:c.992G>A	NP_758526.1:p.Arg331Gln
NR_051953.2:n.2037G>A
NM_002399.4:c.992G>A	NP_002390.1:p.Arg331Gln
NM_172316.3:c.767G>A	NP_758527.1:p.Arg256Gln