Canonical Allele Identifier: CA7469383

Gene: MEIS2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.37094545A>G , CM000677.2:g.37094545A>G	GRCh38
NC_000015.9:g.37386746A>G , CM000677.1:g.37386746A>G	GRCh37
NC_000015.8:g.35174038A>G	NCBI36
NG_029108.1:g.11755T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_170675.5:c.471T>C MANE Select	NP_733775.1:p.His157=
ENST00000561208.6:c.471T>C MANE Select	ENSP00000453793.1:p.His157=
NM_001220482.1:c.471T>C	NP_001207411.1:p.His157=
NM_001220482.2:c.471T>C	NP_001207411.1:p.His157=
NM_002399.3:c.432T>C	NP_002390.1:p.His144=
NM_002399.4:c.432T>C	NP_002390.1:p.His144=
NM_170674.4:c.471T>C	NP_733774.1:p.His157=
NM_170674.5:c.471T>C	NP_733774.1:p.His157=
NM_170675.4:c.471T>C	NP_733775.1:p.His157=
NM_170676.4:c.471T>C	NP_733776.1:p.His157=
NM_170676.5:c.471T>C	NP_733776.1:p.His157=
NM_170677.4:c.471T>C	NP_733777.1:p.His157=
NM_170677.5:c.471T>C	NP_733777.1:p.His157=
NM_172315.2:c.432T>C	NP_758526.1:p.His144=
NM_172315.3:c.432T>C	NP_758526.1:p.His144=
NM_172316.2:c.207T>C	NP_758527.1:p.His69=
NM_172316.3:c.207T>C	NP_758527.1:p.His69=
NR_051953.1:n.1145T>C
NR_051953.2:n.1554T>C
ENST00000314177.12:c.471T>C	ENSP00000326296.8:p.His157=
ENST00000338564.9:c.471T>C	ENSP00000341400.4:p.His157=
ENST00000340545.9:c.432T>C	ENSP00000339549.5:p.His144=
ENST00000397620.6:c.207T>C	ENSP00000380745.2:p.His69=
ENST00000397624.7:c.207T>C	ENSP00000380749.3:p.His69=
ENST00000424352.6:c.471T>C	ENSP00000404185.2:p.His157=
ENST00000557796.6:c.432T>C	ENSP00000452693.2:p.His144=
ENST00000558313.5:c.207T>C	ENSP00000453782.2:p.His69=
ENST00000559085.5:c.432T>C	ENSP00000453390.1:p.His144=
ENST00000559129.1:n.523T>C
ENST00000559129.2:n.523T>C
ENST00000559561.5:c.471T>C	ENSP00000453497.1:p.His157=
ENST00000560570.5:c.*32T>C	ENSP00000453481.1:n.*32T>C
ENST00000560617.5:c.33T>C	ENSP00000452874.1:p.His11=
ENST00000560697.5:c.33T>C	ENSP00000452770.1:p.His11=
ENST00000561163.5:n.791T>C
ENST00000561208.5:c.471T>C	ENSP00000453793.1:p.His157=
ENST00000606653.5:c.21T>C	ENSP00000475660.1:p.His7=
ENST00000607277.5:c.48T>C	ENSP00000475899.1:p.His16=
ENST00000699903.1:c.432T>C	ENSP00000514679.1:p.His144=
ENST00000699904.1:c.432T>C	ENSP00000514680.1:p.His144=
ENST00000699905.1:n.145T>C
ENST00000699955.1:c.471T>C	ENSP00000514715.1:p.His157=
ENST00000699956.1:c.33T>C	ENSP00000514716.1:p.His11=
ENST00000699957.1:n.131T>C
XM_006720522.2:c.471T>C	XP_006720585.1:p.His157=
XM_006720523.1:c.468T>C	XP_006720586.1:p.His156=
XM_006720524.1:c.468T>C	XP_006720587.1:p.His156=
XM_006720525.1:c.468T>C	XP_006720588.1:p.His156=
XM_006720526.2:c.207T>C	XP_006720589.1:p.His69=
XM_006720526.3:c.207T>C	XP_006720589.1:p.His69=
XM_006720527.2:c.33T>C	XP_006720590.1:p.His11=
XM_006720527.3:c.33T>C	XP_006720590.1:p.His11=
XM_006720528.2:c.33T>C	XP_006720591.1:p.His11=
XM_006720529.2:c.33T>C	XP_006720592.1:p.His11=
XM_006720529.3:c.33T>C	XP_006720592.1:p.His11=
XM_011521591.1:c.33T>C	XP_011519893.1:p.His11=
XM_011521591.2:c.33T>C	XP_011519893.1:p.His11=
XM_017022205.2:c.207T>C	XP_016877694.1:p.His69=
XM_024449925.1:c.432T>C	XP_024305693.1:p.His144=
XM_024449926.1:c.432T>C	XP_024305694.1:p.His144=
XM_024449927.1:c.432T>C	XP_024305695.1:p.His144=
XM_024449928.1:c.207T>C	XP_024305696.1:p.His69=
XM_024449929.1:c.432T>C	XP_024305697.1:p.His144=
XR_001751290.2:n.906T>C
XR_002957640.1:n.859T>C
XR_002957641.1:n.859T>C