Canonical Allele Identifier: CA1257754895

Gene: MEIS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66554291_66554292delinsCT , CM000664.2:g.66554291_66554292delinsCT	GRCh38
NC_000002.11:g.66781423_66781424delinsCT , CM000664.1:g.66781423_66781424delinsCT	GRCh37
NC_000002.10:g.66634927_66634928delinsCT	NCBI36
NG_011467.1:g.123892_123893delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272369.14:c.965+6272_965+6273delinsCT MANE Select	ENSP00000272369.8:n.965+6272_965+6273delinsCT
ENST00000272369.13:c.965+6272_965+6273delinsCT	ENSP00000272369.8:n.965+6272_965+6273delinsCT
ENST00000398506.6:c.959+6272_959+6273delinsCT	ENSP00000381518.2:n.959+6272_959+6273delinsCT
ENST00000409517.5:n.279+6272_279+6273delinsCT
ENST00000450027.2:n.420+6272_420+6273delinsCT
ENST00000475239.5:n.525+6272_525+6273delinsCT
ENST00000488550.5:c.965+6272_965+6273delinsCT	ENSP00000475161.1:n.965+6272_965+6273delinsCT
ENST00000495021.6:c.770+6272_770+6273delinsCT	ENSP00000440571.1:n.770+6272_770+6273delinsCT
ENST00000542964.5:n.398+6272_398+6273delinsCT
ENST00000560281.6:c.965+6272_965+6273delinsCT	ENSP00000454209.1:n.965+6272_965+6273delinsCT
ENST00000606455.5:n.419+6272_419+6273delinsCT
NM_002398.2:c.965+6272_965+6273delinsCT	NP_002389.1:n.965+6272_965+6273delinsCT
XM_005264321.1:c.1013+6272_1013+6273delinsCT	XP_005264378.1:n.1013+6272_1013+6273delinsCT
XM_005264322.1:c.965+6272_965+6273delinsCT	XP_005264379.1:n.965+6272_965+6273delinsCT
XM_005264323.1:c.1013+6272_1013+6273delinsCT	XP_005264380.1:n.1013+6272_1013+6273delinsCT
XM_005264324.3:c.770+6272_770+6273delinsCT	XP_005264381.1:n.770+6272_770+6273delinsCT
XM_005264325.3:c.770+6272_770+6273delinsCT	XP_005264382.1:n.770+6272_770+6273delinsCT
XR_244932.1:n.1599+6272_1599+6273delinsCT
XR_244933.1:n.1599+6272_1599+6273delinsCT
NM_002398.3:c.965+6272_965+6273delinsCT MANE Select	NP_002389.1:n.965+6272_965+6273delinsCT