Canonical Allele Identifier: CA347081825

Gene: MEIS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66437762G>A , CM000664.2:g.66437762G>A	GRCh38
NC_000002.11:g.66664894G>A , CM000664.1:g.66664894G>A	GRCh37
NC_000002.10:g.66518398G>A	NCBI36
NG_011467.1:g.7363G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002398.3:c.38G>A MANE Select	NP_002389.1:p.Gly13Asp
ENST00000272369.14:c.38G>A MANE Select	ENSP00000272369.8:p.Gly13Asp
NM_002398.2:c.38G>A	NP_002389.1:p.Gly13Asp
ENST00000272369.13:c.38G>A	ENSP00000272369.8:p.Gly13Asp
ENST00000398506.6:c.32G>A	ENSP00000381518.2:p.Gly11Asp
ENST00000488550.5:c.38G>A	ENSP00000475161.1:p.Gly13Asp
ENST00000490726.2:n.53G>A
ENST00000491706.5:n.726G>A
ENST00000496248.5:n.142G>A
ENST00000560281.6:c.38G>A	ENSP00000454209.1:p.Gly13Asp
XM_005264321.1:c.86G>A	XP_005264378.1:p.Gly29Asp
XM_005264322.1:c.38G>A	XP_005264379.1:p.Gly13Asp
XM_005264323.1:c.86G>A	XP_005264380.1:p.Gly29Asp
XR_244932.1:n.818G>A
XR_244933.1:n.818G>A