Canonical Allele Identifier: CA1257754755

Gene: MEIS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66553943_66553944delinsAT , CM000664.2:g.66553943_66553944delinsAT	GRCh38
NC_000002.11:g.66781075_66781076delinsAT , CM000664.1:g.66781075_66781076delinsAT	GRCh37
NC_000002.10:g.66634579_66634580delinsAT	NCBI36
NG_011467.1:g.123544_123545delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272369.14:c.965+5924_965+5925delinsAT MANE Select	ENSP00000272369.8:n.965+5924_965+5925delinsAT
ENST00000272369.13:c.965+5924_965+5925delinsAT	ENSP00000272369.8:n.965+5924_965+5925delinsAT
ENST00000398506.6:c.959+5924_959+5925delinsAT	ENSP00000381518.2:n.959+5924_959+5925delinsAT
ENST00000409517.5:n.279+5924_279+5925delinsAT
ENST00000450027.2:n.420+5924_420+5925delinsAT
ENST00000475239.5:n.525+5924_525+5925delinsAT
ENST00000488550.5:c.965+5924_965+5925delinsAT	ENSP00000475161.1:n.965+5924_965+5925delinsAT
ENST00000495021.6:c.770+5924_770+5925delinsAT	ENSP00000440571.1:n.770+5924_770+5925delinsAT
ENST00000542964.5:n.398+5924_398+5925delinsAT
ENST00000560281.6:c.965+5924_965+5925delinsAT	ENSP00000454209.1:n.965+5924_965+5925delinsAT
ENST00000606455.5:n.419+5924_419+5925delinsAT
NM_002398.2:c.965+5924_965+5925delinsAT	NP_002389.1:n.965+5924_965+5925delinsAT
XM_005264321.1:c.1013+5924_1013+5925delinsAT	XP_005264378.1:n.1013+5924_1013+5925delinsAT
XM_005264322.1:c.965+5924_965+5925delinsAT	XP_005264379.1:n.965+5924_965+5925delinsAT
XM_005264323.1:c.1013+5924_1013+5925delinsAT	XP_005264380.1:n.1013+5924_1013+5925delinsAT
XM_005264324.3:c.770+5924_770+5925delinsAT	XP_005264381.1:n.770+5924_770+5925delinsAT
XM_005264325.3:c.770+5924_770+5925delinsAT	XP_005264382.1:n.770+5924_770+5925delinsAT
XR_244932.1:n.1599+5924_1599+5925delinsAT
XR_244933.1:n.1599+5924_1599+5925delinsAT
NM_002398.3:c.965+5924_965+5925delinsAT MANE Select	NP_002389.1:n.965+5924_965+5925delinsAT