Canonical Allele Identifier: CA391926972

Gene: MEIS2

Linked Data

• MyVariant Identifiers: chr15:g.37188879T>G (hg19) ; chr15:g.36896678T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36896678T>G , CM000677.2:g.36896678T>G	GRCh38
NC_000015.9:g.37188879T>G , CM000677.1:g.37188879T>G	GRCh37
NC_000015.8:g.34976171T>G	NCBI36
NG_029108.1:g.209622A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699898.1:n.169A>C
ENST00000699899.1:n.169A>C
ENST00000699900.1:n.219A>C
ENST00000699901.1:n.309A>C
ENST00000699902.1:n.149A>C
ENST00000699903.1:c.947A>C	ENSP00000514679.1:p.Asn316Thr
ENST00000699904.1:c.1088A>C	ENSP00000514680.1:p.Asn363Thr
ENST00000699905.1:n.660A>C
ENST00000699906.1:n.213A>C
ENST00000699955.1:c.*197A>C	ENSP00000514715.1:n.*197A>C
ENST00000699956.1:c.548A>C	ENSP00000514716.1:p.Asn183Thr
ENST00000561208.6:c.986A>C MANE Select	ENSP00000453793.1:p.Asn329Thr
ENST00000314177.12:c.909A>C	ENSP00000326296.8:p.Ter303Tyr
ENST00000338564.9:c.986A>C	ENSP00000341400.4:p.Asn329Thr
ENST00000340545.9:c.947A>C	ENSP00000339549.5:p.Asn316Thr
ENST00000397620.6:c.722A>C	ENSP00000380745.2:p.Asn241Thr
ENST00000397624.7:c.722A>C	ENSP00000380749.3:p.Asn241Thr
ENST00000424352.6:c.986A>C	ENSP00000404185.2:p.Asn329Thr
ENST00000557796.6:c.947A>C	ENSP00000452693.2:p.Asn316Thr
ENST00000558643.1:n.473A>C
ENST00000559085.5:c.947A>C	ENSP00000453390.1:p.Asn316Thr
ENST00000559371.5:n.357+42A>C
ENST00000559408.1:n.392A>C
ENST00000559561.5:c.986A>C	ENSP00000453497.1:p.Asn329Thr
ENST00000560570.5:c.*547A>C	ENSP00000453481.1:n.*547A>C
ENST00000560702.1:n.1662A>C
ENST00000561208.5:c.986A>C	ENSP00000453793.1:p.Asn329Thr
ENST00000561284.5:n.81A>C
ENST00000607277.5:c.563A>C	ENSP00000475899.1:p.Asn188Thr
NM_001220482.1:c.986A>C	NP_001207411.1:p.Asn329Thr
NM_002399.3:c.947A>C	NP_002390.1:p.Asn316Thr
NM_170674.4:c.986A>C	NP_733774.1:p.Asn329Thr
NM_170675.4:c.986A>C	NP_733775.1:p.Asn329Thr
NM_170676.4:c.986A>C	NP_733776.1:p.Asn329Thr
NM_170677.4:c.986A>C	NP_733777.1:p.Asn329Thr
NM_172315.2:c.947A>C	NP_758526.1:p.Asn316Thr
NM_172316.2:c.722A>C	NP_758527.1:p.Asn241Thr
NR_051953.1:n.1583A>C
XM_006720522.2:c.986A>C	XP_006720585.1:p.Asn329Thr
XM_006720523.1:c.983A>C	XP_006720586.1:p.Asn328Thr
XM_006720524.1:c.983A>C	XP_006720587.1:p.Asn328Thr
XM_006720525.1:c.983A>C	XP_006720588.1:p.Asn328Thr
XM_006720526.2:c.722A>C	XP_006720589.1:p.Asn241Thr
XM_006720527.2:c.548A>C	XP_006720590.1:p.Asn183Thr
XM_006720528.2:c.548A>C	XP_006720591.1:p.Asn183Thr
XM_006720529.2:c.548A>C	XP_006720592.1:p.Asn183Thr
XM_011521591.1:c.548A>C	XP_011519893.1:p.Asn183Thr
XM_006720526.3:c.722A>C	XP_006720589.1:p.Asn241Thr
XM_006720527.3:c.548A>C	XP_006720590.1:p.Asn183Thr
XM_006720529.3:c.548A>C	XP_006720592.1:p.Asn183Thr
XM_011521591.2:c.548A>C	XP_011519893.1:p.Asn183Thr
XM_017022205.2:c.722A>C	XP_016877694.1:p.Asn241Thr
XM_024449925.1:c.947A>C	XP_024305693.1:p.Asn316Thr
XM_024449926.1:c.947A>C	XP_024305694.1:p.Asn316Thr
XM_024449927.1:c.947A>C	XP_024305695.1:p.Asn316Thr
XM_024449928.1:c.722A>C	XP_024305696.1:p.Asn241Thr
XM_024449929.1:c.947A>C	XP_024305697.1:p.Asn316Thr
XR_001751290.2:n.1344A>C
XR_002957640.1:n.1297A>C
XR_002957641.1:n.1297A>C
NM_170675.5:c.986A>C MANE Select	NP_733775.1:p.Asn329Thr
NM_001220482.2:c.986A>C	NP_001207411.1:p.Asn329Thr
NM_170674.5:c.986A>C	NP_733774.1:p.Asn329Thr
NM_170676.5:c.986A>C	NP_733776.1:p.Asn329Thr
NM_170677.5:c.986A>C	NP_733777.1:p.Asn329Thr
NM_172315.3:c.947A>C	NP_758526.1:p.Asn316Thr
NR_051953.2:n.1992A>C
NM_002399.4:c.947A>C	NP_002390.1:p.Asn316Thr
NM_172316.3:c.722A>C	NP_758527.1:p.Asn241Thr