Canonical Allele Identifier: CA9539269

Gene: MEIS3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47414755C>T , CM000681.2:g.47414755C>T	GRCh38
NC_000019.9:g.47918012C>T , CM000681.1:g.47918012C>T	GRCh37
NC_000019.8:g.52609824C>T	NCBI36
NG_051644.1:g.12479G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558555.6:c.559G>A MANE Select	ENSP00000454073.1:p.Glu187Lys
ENST00000331559.9:c.508G>A	ENSP00000333552.4:p.Glu170Lys
ENST00000441740.6:c.508G>A	ENSP00000388667.2:p.Glu170Lys
ENST00000558555.5:c.559G>A	ENSP00000454073.1:p.Glu187Lys
ENST00000559338.1:c.135G>A
ENST00000559524.5:c.559G>A	ENSP00000452854.1:p.Glu187Lys
ENST00000560245.5:c.184G>A	ENSP00000453757.2:p.Glu62Lys
ENST00000561096.5:c.823G>A	ENSP00000453934.1:p.Glu275Lys
ENST00000561204.5:n.1179G>A
ENST00000561293.5:c.559G>A	ENSP00000453307.1:p.Glu187Lys
NM_001009813.2:c.508G>A	NP_001009813.1:p.Glu170Lys
NM_001301059.1:c.559G>A	NP_001287988.1:p.Glu187Lys
NM_020160.2:c.559G>A	NP_064545.1:p.Glu187Lys
XM_011527136.1:c.772G>A	XP_011525438.1:p.Glu258Lys
XM_011527137.1:c.721G>A	XP_011525439.1:p.Glu241Lys
XM_011527138.1:c.660+1897G>A	XP_011525440.1:n.660+1897G>A
XM_011527139.1:c.550G>A	XP_011525441.1:p.Glu184Lys
XM_011527140.1:c.163G>A	XP_011525442.1:p.Glu55Lys
NM_001346148.1:c.550G>A	NP_001333077.1:p.Glu184Lys
XM_011527136.3:c.772G>A	XP_011525438.1:p.Glu258Lys
XM_017027011.1:c.823G>A	XP_016882500.1:p.Glu275Lys
XM_024451612.1:c.823G>A	XP_024307380.1:p.Glu275Lys
XM_024451613.1:c.772G>A	XP_024307381.1:p.Glu258Lys
XM_024451614.1:c.660+1897G>A	XP_024307382.1:n.660+1897G>A
XM_024451615.1:c.550G>A	XP_024307383.1:p.Glu184Lys
XM_024451616.1:c.508G>A	XP_024307384.1:p.Glu170Lys
XM_024451617.1:c.163G>A	XP_024307385.1:p.Glu55Lys
NM_001009813.3:c.508G>A	NP_001009813.1:p.Glu170Lys
NM_001301059.2:c.559G>A MANE Select	NP_001287988.1:p.Glu187Lys
NM_020160.3:c.559G>A	NP_064545.1:p.Glu187Lys
NM_001346148.2:c.550G>A	NP_001333077.1:p.Glu184Lys