Canonical Allele Identifier: CA1257745153

Gene: MEIS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66531375_66531377delinsGTC , CM000664.2:g.66531375_66531377delinsGTC	GRCh38
NC_000002.11:g.66758507_66758509delinsGTC , CM000664.1:g.66758507_66758509delinsGTC	GRCh37
NC_000002.10:g.66612011_66612013delinsGTC	NCBI36
NG_011467.1:g.100976_100978delinsGTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000272369.14:c.889-16568_889-16566delinsGTC MANE Select	ENSP00000272369.8:n.889-16568_889-16566delinsGTC
ENST00000272369.13:c.889-16568_889-16566delinsGTC	ENSP00000272369.8:n.889-16568_889-16566delinsGTC
ENST00000398506.6:c.883-16568_883-16566delinsGTC	ENSP00000381518.2:n.883-16568_883-16566delinsGTC
ENST00000409517.5:n.203-16568_203-16566delinsGTC
ENST00000450027.2:n.344-16568_344-16566delinsGTC
ENST00000475239.5:n.449-16568_449-16566delinsGTC
ENST00000488550.5:c.889-16568_889-16566delinsGTC	ENSP00000475161.1:n.889-16568_889-16566delinsGTC
ENST00000495021.6:c.694-16568_694-16566delinsGTC	ENSP00000440571.1:n.694-16568_694-16566delinsGTC
ENST00000542964.5:n.322-16568_322-16566delinsGTC
ENST00000560281.6:c.889-16568_889-16566delinsGTC	ENSP00000454209.1:n.889-16568_889-16566delinsGTC
ENST00000606455.5:n.343-16568_343-16566delinsGTC
NM_002398.2:c.889-16568_889-16566delinsGTC	NP_002389.1:n.889-16568_889-16566delinsGTC
XM_005264321.1:c.937-16568_937-16566delinsGTC	XP_005264378.1:n.937-16568_937-16566delinsGTC
XM_005264322.1:c.889-16568_889-16566delinsGTC	XP_005264379.1:n.889-16568_889-16566delinsGTC
XM_005264323.1:c.937-16568_937-16566delinsGTC	XP_005264380.1:n.937-16568_937-16566delinsGTC
XM_005264324.3:c.694-16568_694-16566delinsGTC	XP_005264381.1:n.694-16568_694-16566delinsGTC
XM_005264325.3:c.694-16568_694-16566delinsGTC	XP_005264382.1:n.694-16568_694-16566delinsGTC
XR_244932.1:n.1523-16568_1523-16566delinsGTC
XR_244933.1:n.1523-16568_1523-16566delinsGTC
NM_002398.3:c.889-16568_889-16566delinsGTC MANE Select	NP_002389.1:n.889-16568_889-16566delinsGTC