Canonical Allele Identifier: CA2170135772

Gene: MEIS2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36896702G= , CM000677.2:g.36896702G=	GRCh38
NC_000015.9:g.37188903G= , CM000677.1:g.37188903G=	GRCh37
NC_000015.8:g.34976195G=	NCBI36
NG_029108.1:g.209598C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699898.1:n.161-16C=
ENST00000699899.1:n.161-16C=
ENST00000699900.1:n.211-16C=
ENST00000699901.1:n.301-16C=
ENST00000699902.1:n.141-16C=
ENST00000699903.1:c.939-16C=	ENSP00000514679.1:n.939-16C=
ENST00000699904.1:c.1080-16C=	ENSP00000514680.1:n.1080-16C=
ENST00000699905.1:n.652-16C=
ENST00000699906.1:n.205-16C=
ENST00000699955.1:c.*189-16C=	ENSP00000514715.1:n.*189-16C=
ENST00000699956.1:c.540-16C=	ENSP00000514716.1:n.540-16C=
ENST00000561208.6:c.978-16C= MANE Select	ENSP00000453793.1:n.978-16C=
ENST00000314177.12:c.901-16C=	ENSP00000326296.8:n.901-16C=
ENST00000338564.9:c.978-16C=	ENSP00000341400.4:n.978-16C=
ENST00000340545.9:c.939-16C=	ENSP00000339549.5:n.939-16C=
ENST00000397620.6:c.714-16C=	ENSP00000380745.2:n.714-16C=
ENST00000397624.7:c.714-16C=	ENSP00000380749.3:n.714-16C=
ENST00000424352.6:c.978-16C=	ENSP00000404185.2:n.978-16C=
ENST00000557796.6:c.939-16C=	ENSP00000452693.2:n.939-16C=
ENST00000558643.1:n.449C=
ENST00000559085.5:c.939-16C=	ENSP00000453390.1:n.939-16C=
ENST00000559371.5:n.357+18C=
ENST00000559408.1:n.384-16C=
ENST00000559561.5:c.978-16C=	ENSP00000453497.1:n.978-16C=
ENST00000560570.5:c.*539-16C=	ENSP00000453481.1:n.*539-16C=
ENST00000560702.1:n.1638C=
ENST00000561208.5:c.978-16C=	ENSP00000453793.1:n.978-16C=
ENST00000561284.5:n.73-16C=
ENST00000607277.5:c.555-16C=	ENSP00000475899.1:n.555-16C=
NM_001220482.1:c.978-16C=	NP_001207411.1:n.978-16C=
NM_002399.3:c.939-16C=	NP_002390.1:n.939-16C=
NM_170674.4:c.978-16C=	NP_733774.1:n.978-16C=
NM_170675.4:c.978-16C=	NP_733775.1:n.978-16C=
NM_170676.4:c.978-16C=	NP_733776.1:n.978-16C=
NM_170677.4:c.978-16C=	NP_733777.1:n.978-16C=
NM_172315.2:c.939-16C=	NP_758526.1:n.939-16C=
NM_172316.2:c.714-16C=	NP_758527.1:n.714-16C=
NR_051953.1:n.1575-16C=
XM_006720522.2:c.978-16C=	XP_006720585.1:n.978-16C=
XM_006720523.1:c.975-16C=	XP_006720586.1:n.975-16C=
XM_006720524.1:c.975-16C=	XP_006720587.1:n.975-16C=
XM_006720525.1:c.975-16C=	XP_006720588.1:n.975-16C=
XM_006720526.2:c.714-16C=	XP_006720589.1:n.714-16C=
XM_006720527.2:c.540-16C=	XP_006720590.1:n.540-16C=
XM_006720528.2:c.540-16C=	XP_006720591.1:n.540-16C=
XM_006720529.2:c.540-16C=	XP_006720592.1:n.540-16C=
XM_011521591.1:c.540-16C=	XP_011519893.1:n.540-16C=
XM_006720526.3:c.714-16C=	XP_006720589.1:n.714-16C=
XM_006720527.3:c.540-16C=	XP_006720590.1:n.540-16C=
XM_006720529.3:c.540-16C=	XP_006720592.1:n.540-16C=
XM_011521591.2:c.540-16C=	XP_011519893.1:n.540-16C=
XM_017022205.2:c.714-16C=	XP_016877694.1:n.714-16C=
XM_024449925.1:c.939-16C=	XP_024305693.1:n.939-16C=
XM_024449926.1:c.939-16C=	XP_024305694.1:n.939-16C=
XM_024449927.1:c.939-16C=	XP_024305695.1:n.939-16C=
XM_024449928.1:c.714-16C=	XP_024305696.1:n.714-16C=
XM_024449929.1:c.939-16C=	XP_024305697.1:n.939-16C=
XR_001751290.2:n.1336-16C=
XR_002957640.1:n.1289-16C=
XR_002957641.1:n.1289-16C=
NM_170675.5:c.978-16C= MANE Select	NP_733775.1:n.978-16C=
NM_001220482.2:c.978-16C=	NP_001207411.1:n.978-16C=
NM_170674.5:c.978-16C=	NP_733774.1:n.978-16C=
NM_170676.5:c.978-16C=	NP_733776.1:n.978-16C=
NM_170677.5:c.978-16C=	NP_733777.1:n.978-16C=
NM_172315.3:c.939-16C=	NP_758526.1:n.939-16C=
NR_051953.2:n.1984-16C=
NM_002399.4:c.939-16C=	NP_002390.1:n.939-16C=
NM_172316.3:c.714-16C=	NP_758527.1:n.714-16C=