Canonical Allele Identifier: CA347082879

Gene: MEIS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66441435T>A , CM000664.2:g.66441435T>A	GRCh38
NC_000002.11:g.66668567T>A , CM000664.1:g.66668567T>A	GRCh37
NC_000002.10:g.66522071T>A	NCBI36
NG_011467.1:g.11036T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272369.14:c.454T>A MANE Select	ENSP00000272369.8:p.Leu152Ile
ENST00000272369.13:c.454T>A	ENSP00000272369.8:p.Leu152Ile
ENST00000398506.6:c.448T>A	ENSP00000381518.2:p.Leu150Ile
ENST00000409622.5:n.249+1090T>A
ENST00000437869.1:c.75T>A
ENST00000466811.2:n.323T>A
ENST00000488550.5:c.454T>A	ENSP00000475161.1:p.Leu152Ile
ENST00000490726.2:n.469T>A
ENST00000491706.5:n.1000T>A
ENST00000495021.6:c.259T>A	ENSP00000440571.1:p.Leu87Ile
ENST00000560281.6:c.454T>A	ENSP00000454209.1:p.Leu152Ile
NM_002398.2:c.454T>A	NP_002389.1:p.Leu152Ile
XM_005264321.1:c.502T>A	XP_005264378.1:p.Leu168Ile
XM_005264322.1:c.454T>A	XP_005264379.1:p.Leu152Ile
XM_005264323.1:c.502T>A	XP_005264380.1:p.Leu168Ile
XM_005264324.3:c.259T>A	XP_005264381.1:p.Leu87Ile
XM_005264325.3:c.259T>A	XP_005264382.1:p.Leu87Ile
XR_244932.1:n.1234T>A
XR_244933.1:n.1234T>A
NM_002398.3:c.454T>A MANE Select	NP_002389.1:p.Leu152Ile