Canonical Allele Identifier: CA2627700667

Gene: MEIS2

Linked Data

• gnomAD v4: 15-36950237-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.36950237T>G , CM000677.2:g.36950237T>G	GRCh38
NC_000015.9:g.37242438T>G , CM000677.1:g.37242438T>G	GRCh37
NC_000015.8:g.35029730T>G	NCBI36
NG_029108.1:g.156063A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000699898.1:n.160+87A>C
ENST00000699899.1:n.160+87A>C
ENST00000699900.1:n.210+87A>C
ENST00000699901.1:n.300+87A>C
ENST00000699902.1:n.140+87A>C
ENST00000699903.1:c.938+87A>C	ENSP00000514679.1:n.938+87A>C
ENST00000699904.1:c.938+87A>C	ENSP00000514680.1:n.938+87A>C
ENST00000699905.1:n.651+87A>C
ENST00000699955.1:c.*188+87A>C	ENSP00000514715.1:n.*188+87A>C
ENST00000699956.1:c.539+87A>C	ENSP00000514716.1:n.539+87A>C
ENST00000561208.6:c.977+87A>C MANE Select	ENSP00000453793.1:n.977+87A>C
ENST00000314177.12:c.901-53551A>C	ENSP00000326296.8:n.901-53551A>C
ENST00000338564.9:c.977+87A>C	ENSP00000341400.4:n.977+87A>C
ENST00000340545.9:c.938+87A>C	ENSP00000339549.5:n.938+87A>C
ENST00000397620.6:c.713+87A>C	ENSP00000380745.2:n.713+87A>C
ENST00000397624.7:c.713+87A>C	ENSP00000380749.3:n.713+87A>C
ENST00000424352.6:c.977+87A>C	ENSP00000404185.2:n.977+87A>C
ENST00000557796.6:c.938+87A>C	ENSP00000452693.2:n.938+87A>C
ENST00000559085.5:c.938+87A>C	ENSP00000453390.1:n.938+87A>C
ENST00000559561.5:c.977+87A>C	ENSP00000453497.1:n.977+87A>C
ENST00000560570.5:c.*538+87A>C	ENSP00000453481.1:n.*538+87A>C
ENST00000561208.5:c.977+87A>C	ENSP00000453793.1:n.977+87A>C
ENST00000607277.5:c.554+87A>C	ENSP00000475899.1:n.554+87A>C
NM_001220482.1:c.977+87A>C	NP_001207411.1:n.977+87A>C
NM_002399.3:c.938+87A>C	NP_002390.1:n.938+87A>C
NM_170674.4:c.977+87A>C	NP_733774.1:n.977+87A>C
NM_170675.4:c.977+87A>C	NP_733775.1:n.977+87A>C
NM_170676.4:c.977+87A>C	NP_733776.1:n.977+87A>C
NM_170677.4:c.977+87A>C	NP_733777.1:n.977+87A>C
NM_172315.2:c.938+87A>C	NP_758526.1:n.938+87A>C
NM_172316.2:c.713+87A>C	NP_758527.1:n.713+87A>C
NR_051953.1:n.1575-53551A>C
XM_006720522.2:c.977+87A>C	XP_006720585.1:n.977+87A>C
XM_006720523.1:c.974+87A>C	XP_006720586.1:n.974+87A>C
XM_006720524.1:c.974+87A>C	XP_006720587.1:n.974+87A>C
XM_006720525.1:c.974+87A>C	XP_006720588.1:n.974+87A>C
XM_006720526.2:c.713+87A>C	XP_006720589.1:n.713+87A>C
XM_006720527.2:c.539+87A>C	XP_006720590.1:n.539+87A>C
XM_006720528.2:c.539+87A>C	XP_006720591.1:n.539+87A>C
XM_006720529.2:c.539+87A>C	XP_006720592.1:n.539+87A>C
XM_011521591.1:c.539+87A>C	XP_011519893.1:n.539+87A>C
XM_006720526.3:c.713+87A>C	XP_006720589.1:n.713+87A>C
XM_006720527.3:c.539+87A>C	XP_006720590.1:n.539+87A>C
XM_006720529.3:c.539+87A>C	XP_006720592.1:n.539+87A>C
XM_011521591.2:c.539+87A>C	XP_011519893.1:n.539+87A>C
XM_017022205.2:c.713+87A>C	XP_016877694.1:n.713+87A>C
XM_024449925.1:c.938+87A>C	XP_024305693.1:n.938+87A>C
XM_024449926.1:c.938+87A>C	XP_024305694.1:n.938+87A>C
XM_024449927.1:c.938+87A>C	XP_024305695.1:n.938+87A>C
XM_024449928.1:c.713+87A>C	XP_024305696.1:n.713+87A>C
XM_024449929.1:c.938+87A>C	XP_024305697.1:n.938+87A>C
XR_001751290.2:n.1336-53551A>C
XR_002957640.1:n.1289-53551A>C
XR_002957641.1:n.1289-53551A>C
NM_170675.5:c.977+87A>C MANE Select	NP_733775.1:n.977+87A>C
NM_001220482.2:c.977+87A>C	NP_001207411.1:n.977+87A>C
NM_170674.5:c.977+87A>C	NP_733774.1:n.977+87A>C
NM_170676.5:c.977+87A>C	NP_733776.1:n.977+87A>C
NM_170677.5:c.977+87A>C	NP_733777.1:n.977+87A>C
NM_172315.3:c.938+87A>C	NP_758526.1:n.938+87A>C
NR_051953.2:n.1984-53551A>C
NM_002399.4:c.938+87A>C	NP_002390.1:n.938+87A>C
NM_172316.3:c.713+87A>C	NP_758527.1:n.713+87A>C