Canonical Allele Identifier: CA391926923

Gene: MEIS2

Linked Data

• MyVariant Identifiers: chr15:g.37188858T>C (hg19) ; chr15:g.36896657T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36896657T>C , CM000677.2:g.36896657T>C	GRCh38
NC_000015.9:g.37188858T>C , CM000677.1:g.37188858T>C	GRCh37
NC_000015.8:g.34976150T>C	NCBI36
NG_029108.1:g.209643A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699898.1:n.190A>G
ENST00000699899.1:n.190A>G
ENST00000699900.1:n.240A>G
ENST00000699901.1:n.330A>G
ENST00000699902.1:n.170A>G
ENST00000699903.1:c.968A>G	ENSP00000514679.1:p.Gln323Arg
ENST00000699904.1:c.1109A>G	ENSP00000514680.1:p.Gln370Arg
ENST00000699905.1:n.681A>G
ENST00000699906.1:n.234A>G
ENST00000699955.1:c.*218A>G	ENSP00000514715.1:n.*218A>G
ENST00000699956.1:c.569A>G	ENSP00000514716.1:p.Gln190Arg
ENST00000561208.6:c.1007A>G MANE Select	ENSP00000453793.1:p.Gln336Arg
ENST00000314177.12:c.*21A>G	ENSP00000326296.8:n.*21A>G
ENST00000338564.9:c.1007A>G	ENSP00000341400.4:p.Gln336Arg
ENST00000340545.9:c.968A>G	ENSP00000339549.5:p.Gln323Arg
ENST00000397620.6:c.743A>G	ENSP00000380745.2:p.Gln248Arg
ENST00000397624.7:c.743A>G	ENSP00000380749.3:p.Gln248Arg
ENST00000424352.6:c.1007A>G	ENSP00000404185.2:p.Gln336Arg
ENST00000557796.6:c.968A>G	ENSP00000452693.2:p.Gln323Arg
ENST00000558643.1:n.494A>G
ENST00000559085.5:c.968A>G	ENSP00000453390.1:p.Gln323Arg
ENST00000559371.5:n.357+63A>G
ENST00000559408.1:n.413A>G
ENST00000559561.5:c.1007A>G	ENSP00000453497.1:p.Gln336Arg
ENST00000560570.5:c.*568A>G	ENSP00000453481.1:n.*568A>G
ENST00000560702.1:n.1683A>G
ENST00000561208.5:c.1007A>G	ENSP00000453793.1:p.Gln336Arg
ENST00000561284.5:n.102A>G
ENST00000607277.5:c.584A>G	ENSP00000475899.1:p.Gln195Arg
NM_001220482.1:c.1007A>G	NP_001207411.1:p.Gln336Arg
NM_002399.3:c.968A>G	NP_002390.1:p.Gln323Arg
NM_170674.4:c.1007A>G	NP_733774.1:p.Gln336Arg
NM_170675.4:c.1007A>G	NP_733775.1:p.Gln336Arg
NM_170676.4:c.1007A>G	NP_733776.1:p.Gln336Arg
NM_170677.4:c.1007A>G	NP_733777.1:p.Gln336Arg
NM_172315.2:c.968A>G	NP_758526.1:p.Gln323Arg
NM_172316.2:c.743A>G	NP_758527.1:p.Gln248Arg
NR_051953.1:n.1604A>G
XM_006720522.2:c.1007A>G	XP_006720585.1:p.Gln336Arg
XM_006720523.1:c.1004A>G	XP_006720586.1:p.Gln335Arg
XM_006720524.1:c.1004A>G	XP_006720587.1:p.Gln335Arg
XM_006720525.1:c.1004A>G	XP_006720588.1:p.Gln335Arg
XM_006720526.2:c.743A>G	XP_006720589.1:p.Gln248Arg
XM_006720527.2:c.569A>G	XP_006720590.1:p.Gln190Arg
XM_006720528.2:c.569A>G	XP_006720591.1:p.Gln190Arg
XM_006720529.2:c.569A>G	XP_006720592.1:p.Gln190Arg
XM_011521591.1:c.569A>G	XP_011519893.1:p.Gln190Arg
XM_006720526.3:c.743A>G	XP_006720589.1:p.Gln248Arg
XM_006720527.3:c.569A>G	XP_006720590.1:p.Gln190Arg
XM_006720529.3:c.569A>G	XP_006720592.1:p.Gln190Arg
XM_011521591.2:c.569A>G	XP_011519893.1:p.Gln190Arg
XM_017022205.2:c.743A>G	XP_016877694.1:p.Gln248Arg
XM_024449925.1:c.968A>G	XP_024305693.1:p.Gln323Arg
XM_024449926.1:c.968A>G	XP_024305694.1:p.Gln323Arg
XM_024449927.1:c.968A>G	XP_024305695.1:p.Gln323Arg
XM_024449928.1:c.743A>G	XP_024305696.1:p.Gln248Arg
XM_024449929.1:c.968A>G	XP_024305697.1:p.Gln323Arg
XR_001751290.2:n.1365A>G
XR_002957640.1:n.1318A>G
XR_002957641.1:n.1318A>G
NM_170675.5:c.1007A>G MANE Select	NP_733775.1:p.Gln336Arg
NM_001220482.2:c.1007A>G	NP_001207411.1:p.Gln336Arg
NM_170674.5:c.1007A>G	NP_733774.1:p.Gln336Arg
NM_170676.5:c.1007A>G	NP_733776.1:p.Gln336Arg
NM_170677.5:c.1007A>G	NP_733777.1:p.Gln336Arg
NM_172315.3:c.968A>G	NP_758526.1:p.Gln323Arg
NR_051953.2:n.2013A>G
NM_002399.4:c.968A>G	NP_002390.1:p.Gln323Arg
NM_172316.3:c.743A>G	NP_758527.1:p.Gln248Arg