Canonical Allele Identifier: CA269132323

Gene: MEIS2

Linked Data

• dbSNP Id: rs11293336
• gnomAD v2: 15-37242440-GAA-G
• gnomAD v3: 15-36950239-GAA-G
• gnomAD v4: 15-36950239-GAA-G
• MyVariant Identifiers: chr15:g.37242441_37242442del (hg19) ; chr15:g.36950240_36950241del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36950252_36950253del , CM000677.2:g.36950252_36950253del	GRCh38
NC_000015.9:g.37242453_37242454del , CM000677.1:g.37242453_37242454del	GRCh37
NC_000015.8:g.35029745_35029746del	NCBI36
NG_029108.1:g.156059_156060del

Transcript Alleles

HGVS	Amino-acid change
ENST00000699898.1:n.160+83_160+84del
ENST00000699899.1:n.160+83_160+84del
ENST00000699900.1:n.210+83_210+84del
ENST00000699901.1:n.300+83_300+84del
ENST00000699902.1:n.140+83_140+84del
ENST00000699903.1:c.938+83_938+84del	ENSP00000514679.1:n.938+83_938+84del
ENST00000699904.1:c.938+83_938+84del	ENSP00000514680.1:n.938+83_938+84del
ENST00000699905.1:n.651+83_651+84del
ENST00000699955.1:c.*188+83_*188+84del	ENSP00000514715.1:n.*188+83_*188+84del
ENST00000699956.1:c.539+83_539+84del	ENSP00000514716.1:n.539+83_539+84del
ENST00000561208.6:c.977+83_977+84del MANE Select	ENSP00000453793.1:n.977+83_977+84del
ENST00000314177.12:c.901-53555_901-53554del	ENSP00000326296.8:n.901-53555_901-53554de...
ENST00000338564.9:c.977+83_977+84del	ENSP00000341400.4:n.977+83_977+84del
ENST00000340545.9:c.938+83_938+84del	ENSP00000339549.5:n.938+83_938+84del
ENST00000397620.6:c.713+83_713+84del	ENSP00000380745.2:n.713+83_713+84del
ENST00000397624.7:c.713+83_713+84del	ENSP00000380749.3:n.713+83_713+84del
ENST00000424352.6:c.977+83_977+84del	ENSP00000404185.2:n.977+83_977+84del
ENST00000557796.6:c.938+83_938+84del	ENSP00000452693.2:n.938+83_938+84del
ENST00000559085.5:c.938+83_938+84del	ENSP00000453390.1:n.938+83_938+84del
ENST00000559561.5:c.977+83_977+84del	ENSP00000453497.1:n.977+83_977+84del
ENST00000560570.5:c.*538+83_*538+84del	ENSP00000453481.1:n.*538+83_*538+84del
ENST00000561208.5:c.977+83_977+84del	ENSP00000453793.1:n.977+83_977+84del
ENST00000607277.5:c.554+83_554+84del	ENSP00000475899.1:n.554+83_554+84del
NM_001220482.1:c.977+83_977+84del	NP_001207411.1:n.977+83_977+84del
NM_002399.3:c.938+83_938+84del	NP_002390.1:n.938+83_938+84del
NM_170674.4:c.977+83_977+84del	NP_733774.1:n.977+83_977+84del
NM_170675.4:c.977+83_977+84del	NP_733775.1:n.977+83_977+84del
NM_170676.4:c.977+83_977+84del	NP_733776.1:n.977+83_977+84del
NM_170677.4:c.977+83_977+84del	NP_733777.1:n.977+83_977+84del
NM_172315.2:c.938+83_938+84del	NP_758526.1:n.938+83_938+84del
NM_172316.2:c.713+83_713+84del	NP_758527.1:n.713+83_713+84del
NR_051953.1:n.1575-53555_1575-53554del
XM_006720522.2:c.977+83_977+84del	XP_006720585.1:n.977+83_977+84del
XM_006720523.1:c.974+83_974+84del	XP_006720586.1:n.974+83_974+84del
XM_006720524.1:c.974+83_974+84del	XP_006720587.1:n.974+83_974+84del
XM_006720525.1:c.974+83_974+84del	XP_006720588.1:n.974+83_974+84del
XM_006720526.2:c.713+83_713+84del	XP_006720589.1:n.713+83_713+84del
XM_006720527.2:c.539+83_539+84del	XP_006720590.1:n.539+83_539+84del
XM_006720528.2:c.539+83_539+84del	XP_006720591.1:n.539+83_539+84del
XM_006720529.2:c.539+83_539+84del	XP_006720592.1:n.539+83_539+84del
XM_011521591.1:c.539+83_539+84del	XP_011519893.1:n.539+83_539+84del
XM_006720526.3:c.713+83_713+84del	XP_006720589.1:n.713+83_713+84del
XM_006720527.3:c.539+83_539+84del	XP_006720590.1:n.539+83_539+84del
XM_006720529.3:c.539+83_539+84del	XP_006720592.1:n.539+83_539+84del
XM_011521591.2:c.539+83_539+84del	XP_011519893.1:n.539+83_539+84del
XM_017022205.2:c.713+83_713+84del	XP_016877694.1:n.713+83_713+84del
XM_024449925.1:c.938+83_938+84del	XP_024305693.1:n.938+83_938+84del
XM_024449926.1:c.938+83_938+84del	XP_024305694.1:n.938+83_938+84del
XM_024449927.1:c.938+83_938+84del	XP_024305695.1:n.938+83_938+84del
XM_024449928.1:c.713+83_713+84del	XP_024305696.1:n.713+83_713+84del
XM_024449929.1:c.938+83_938+84del	XP_024305697.1:n.938+83_938+84del
XR_001751290.2:n.1336-53555_1336-53554del
XR_002957640.1:n.1289-53555_1289-53554del
XR_002957641.1:n.1289-53555_1289-53554del
NM_170675.5:c.977+83_977+84del MANE Select	NP_733775.1:n.977+83_977+84del
NM_001220482.2:c.977+83_977+84del	NP_001207411.1:n.977+83_977+84del
NM_170674.5:c.977+83_977+84del	NP_733774.1:n.977+83_977+84del
NM_170676.5:c.977+83_977+84del	NP_733776.1:n.977+83_977+84del
NM_170677.5:c.977+83_977+84del	NP_733777.1:n.977+83_977+84del
NM_172315.3:c.938+83_938+84del	NP_758526.1:n.938+83_938+84del
NR_051953.2:n.1984-53555_1984-53554del
NM_002399.4:c.938+83_938+84del	NP_002390.1:n.938+83_938+84del
NM_172316.3:c.713+83_713+84del	NP_758527.1:n.713+83_713+84del