Canonical Allele Identifier: CA10576003

Gene: MEIS2

Linked Data

• ClinVar Variation Id: 224962
• ClinVar RCV Id: RCV000210625 ; RCV000494204 ; RCV000509419 ; RCV001267141
• dbSNP Id: rs879255264
• MyVariant Identifiers: chr15:g.37188865_37188867del (hg19) ; chr15:g.36896664_36896666del (hg38)
• PubMed: PMID:25712757

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36896671_36896673del , CM000677.2:g.36896671_36896673del	GRCh38
NC_000015.9:g.37188872_37188874del , CM000677.1:g.37188872_37188874del	GRCh37
NC_000015.8:g.34976164_34976166del	NCBI36
NG_029108.1:g.209634_209636del

Transcript Alleles

HGVS	Amino-acid change
ENST00000699898.1:n.181_183del
ENST00000699899.1:n.181_183del
ENST00000699900.1:n.231_233del
ENST00000699901.1:n.321_323del
ENST00000699902.1:n.161_163del
ENST00000699903.1:c.959_961del	ENSP00000514679.1:p.Arg320del
ENST00000699904.1:c.1100_1102del	ENSP00000514680.1:p.Arg367del
ENST00000699905.1:n.672_674del
ENST00000699906.1:n.225_227del
ENST00000699955.1:c.*209_*211del	ENSP00000514715.1:n.*209_*211del
ENST00000699956.1:c.560_562del	ENSP00000514716.1:p.Arg187del
ENST00000561208.6:c.998_1000del MANE Select	ENSP00000453793.1:p.Arg333del
ENST00000314177.12:c.*12_*14del	ENSP00000326296.8:n.*12_*14del
ENST00000338564.9:c.998_1000del	ENSP00000341400.4:p.Arg333del
ENST00000340545.9:c.959_961del	ENSP00000339549.5:p.Arg320del
ENST00000397620.6:c.734_736del	ENSP00000380745.2:p.Arg245del
ENST00000397624.7:c.734_736del	ENSP00000380749.3:p.Arg245del
ENST00000424352.6:c.998_1000del	ENSP00000404185.2:p.Arg333del
ENST00000557796.6:c.959_961del	ENSP00000452693.2:p.Arg320del
ENST00000558643.1:n.485_487del
ENST00000559085.5:c.959_961del	ENSP00000453390.1:p.Arg320del
ENST00000559371.5:n.357+54_357+56del
ENST00000559408.1:n.404_406del
ENST00000559561.5:c.998_1000del	ENSP00000453497.1:p.Arg333del
ENST00000560570.5:c.*559_*561del	ENSP00000453481.1:n.*559_*561del
ENST00000560702.1:n.1674_1676del
ENST00000561208.5:c.998_1000del	ENSP00000453793.1:p.Arg333del
ENST00000561284.5:n.93_95del
ENST00000607277.5:c.575_577del	ENSP00000475899.1:p.Arg192del
NM_001220482.1:c.998_1000del	NP_001207411.1:p.Arg333del
NM_002399.3:c.959_961del	NP_002390.1:p.Arg320del
NM_170674.4:c.998_1000del	NP_733774.1:p.Arg333del
NM_170675.4:c.998_1000del	NP_733775.1:p.Arg333del
NM_170676.4:c.998_1000del	NP_733776.1:p.Arg333del
NM_170677.4:c.998_1000del	NP_733777.1:p.Arg333del
NM_172315.2:c.959_961del	NP_758526.1:p.Arg320del
NM_172316.2:c.734_736del	NP_758527.1:p.Arg245del
NR_051953.1:n.1595_1597del
XM_006720522.2:c.998_1000del	XP_006720585.1:p.Arg333del
XM_006720523.1:c.995_997del	XP_006720586.1:p.Arg332del
XM_006720524.1:c.995_997del	XP_006720587.1:p.Arg332del
XM_006720525.1:c.995_997del	XP_006720588.1:p.Arg332del
XM_006720526.2:c.734_736del	XP_006720589.1:p.Arg245del
XM_006720527.2:c.560_562del	XP_006720590.1:p.Arg187del
XM_006720528.2:c.560_562del	XP_006720591.1:p.Arg187del
XM_006720529.2:c.560_562del	XP_006720592.1:p.Arg187del
XM_011521591.1:c.560_562del	XP_011519893.1:p.Arg187del
XM_006720526.3:c.734_736del	XP_006720589.1:p.Arg245del
XM_006720527.3:c.560_562del	XP_006720590.1:p.Arg187del
XM_006720529.3:c.560_562del	XP_006720592.1:p.Arg187del
XM_011521591.2:c.560_562del	XP_011519893.1:p.Arg187del
XM_017022205.2:c.734_736del	XP_016877694.1:p.Arg245del
XM_024449925.1:c.959_961del	XP_024305693.1:p.Arg320del
XM_024449926.1:c.959_961del	XP_024305694.1:p.Arg320del
XM_024449927.1:c.959_961del	XP_024305695.1:p.Arg320del
XM_024449928.1:c.734_736del	XP_024305696.1:p.Arg245del
XM_024449929.1:c.959_961del	XP_024305697.1:p.Arg320del
XR_001751290.2:n.1356_1358del
XR_002957640.1:n.1309_1311del
XR_002957641.1:n.1309_1311del
NM_170675.5:c.998_1000del MANE Select	NP_733775.1:p.Arg333del
NM_001220482.2:c.998_1000del	NP_001207411.1:p.Arg333del
NM_170674.5:c.998_1000del	NP_733774.1:p.Arg333del
NM_170676.5:c.998_1000del	NP_733776.1:p.Arg333del
NM_170677.5:c.998_1000del	NP_733777.1:p.Arg333del
NM_172315.3:c.959_961del	NP_758526.1:p.Arg320del
NR_051953.2:n.2004_2006del
NM_002399.4:c.959_961del	NP_002390.1:p.Arg320del
NM_172316.3:c.734_736del	NP_758527.1:p.Arg245del