Canonical Allele Identifier: CA391926986

Gene: MEIS2

Linked Data

• MyVariant Identifiers: chr15:g.37188885A>G (hg19) ; chr15:g.36896684A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36896684A>G , CM000677.2:g.36896684A>G	GRCh38
NC_000015.9:g.37188885A>G , CM000677.1:g.37188885A>G	GRCh37
NC_000015.8:g.34976177A>G	NCBI36
NG_029108.1:g.209616T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000699898.1:n.163T>C
ENST00000699899.1:n.163T>C
ENST00000699900.1:n.213T>C
ENST00000699901.1:n.303T>C
ENST00000699902.1:n.143T>C
ENST00000699903.1:c.941T>C	ENSP00000514679.1:p.Phe314Ser
ENST00000699904.1:c.1082T>C	ENSP00000514680.1:p.Phe361Ser
ENST00000699905.1:n.654T>C
ENST00000699906.1:n.207T>C
ENST00000699955.1:c.*191T>C	ENSP00000514715.1:n.*191T>C
ENST00000699956.1:c.542T>C	ENSP00000514716.1:p.Phe181Ser
ENST00000561208.6:c.980T>C MANE Select	ENSP00000453793.1:p.Phe327Ser
ENST00000314177.12:c.903T>C	ENSP00000326296.8:p.Val301=
ENST00000338564.9:c.980T>C	ENSP00000341400.4:p.Phe327Ser
ENST00000340545.9:c.941T>C	ENSP00000339549.5:p.Phe314Ser
ENST00000397620.6:c.716T>C	ENSP00000380745.2:p.Phe239Ser
ENST00000397624.7:c.716T>C	ENSP00000380749.3:p.Phe239Ser
ENST00000424352.6:c.980T>C	ENSP00000404185.2:p.Phe327Ser
ENST00000557796.6:c.941T>C	ENSP00000452693.2:p.Phe314Ser
ENST00000558643.1:n.467T>C
ENST00000559085.5:c.941T>C	ENSP00000453390.1:p.Phe314Ser
ENST00000559371.5:n.357+36T>C
ENST00000559408.1:n.386T>C
ENST00000559561.5:c.980T>C	ENSP00000453497.1:p.Phe327Ser
ENST00000560570.5:c.*541T>C	ENSP00000453481.1:n.*541T>C
ENST00000560702.1:n.1656T>C
ENST00000561208.5:c.980T>C	ENSP00000453793.1:p.Phe327Ser
ENST00000561284.5:n.75T>C
ENST00000607277.5:c.557T>C	ENSP00000475899.1:p.Phe186Ser
NM_001220482.1:c.980T>C	NP_001207411.1:p.Phe327Ser
NM_002399.3:c.941T>C	NP_002390.1:p.Phe314Ser
NM_170674.4:c.980T>C	NP_733774.1:p.Phe327Ser
NM_170675.4:c.980T>C	NP_733775.1:p.Phe327Ser
NM_170676.4:c.980T>C	NP_733776.1:p.Phe327Ser
NM_170677.4:c.980T>C	NP_733777.1:p.Phe327Ser
NM_172315.2:c.941T>C	NP_758526.1:p.Phe314Ser
NM_172316.2:c.716T>C	NP_758527.1:p.Phe239Ser
NR_051953.1:n.1577T>C
XM_006720522.2:c.980T>C	XP_006720585.1:p.Phe327Ser
XM_006720523.1:c.977T>C	XP_006720586.1:p.Phe326Ser
XM_006720524.1:c.977T>C	XP_006720587.1:p.Phe326Ser
XM_006720525.1:c.977T>C	XP_006720588.1:p.Phe326Ser
XM_006720526.2:c.716T>C	XP_006720589.1:p.Phe239Ser
XM_006720527.2:c.542T>C	XP_006720590.1:p.Phe181Ser
XM_006720528.2:c.542T>C	XP_006720591.1:p.Phe181Ser
XM_006720529.2:c.542T>C	XP_006720592.1:p.Phe181Ser
XM_011521591.1:c.542T>C	XP_011519893.1:p.Phe181Ser
XM_006720526.3:c.716T>C	XP_006720589.1:p.Phe239Ser
XM_006720527.3:c.542T>C	XP_006720590.1:p.Phe181Ser
XM_006720529.3:c.542T>C	XP_006720592.1:p.Phe181Ser
XM_011521591.2:c.542T>C	XP_011519893.1:p.Phe181Ser
XM_017022205.2:c.716T>C	XP_016877694.1:p.Phe239Ser
XM_024449925.1:c.941T>C	XP_024305693.1:p.Phe314Ser
XM_024449926.1:c.941T>C	XP_024305694.1:p.Phe314Ser
XM_024449927.1:c.941T>C	XP_024305695.1:p.Phe314Ser
XM_024449928.1:c.716T>C	XP_024305696.1:p.Phe239Ser
XM_024449929.1:c.941T>C	XP_024305697.1:p.Phe314Ser
XR_001751290.2:n.1338T>C
XR_002957640.1:n.1291T>C
XR_002957641.1:n.1291T>C
NM_170675.5:c.980T>C MANE Select	NP_733775.1:p.Phe327Ser
NM_001220482.2:c.980T>C	NP_001207411.1:p.Phe327Ser
NM_170674.5:c.980T>C	NP_733774.1:p.Phe327Ser
NM_170676.5:c.980T>C	NP_733776.1:p.Phe327Ser
NM_170677.5:c.980T>C	NP_733777.1:p.Phe327Ser
NM_172315.3:c.941T>C	NP_758526.1:p.Phe314Ser
NR_051953.2:n.1986T>C
NM_002399.4:c.941T>C	NP_002390.1:p.Phe314Ser
NM_172316.3:c.716T>C	NP_758527.1:p.Phe239Ser