Canonical Allele Identifier: CA1257754857

Gene: MEIS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66554206T= , CM000664.2:g.66554206T=	GRCh38
NC_000002.11:g.66781338T= , CM000664.1:g.66781338T=	GRCh37
NC_000002.10:g.66634842T=	NCBI36
NG_011467.1:g.123807T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272369.14:c.965+6187T= MANE Select	ENSP00000272369.8:n.965+6187T=
ENST00000272369.13:c.965+6187T=	ENSP00000272369.8:n.965+6187T=
ENST00000398506.6:c.959+6187T=	ENSP00000381518.2:n.959+6187T=
ENST00000409517.5:n.279+6187T=
ENST00000450027.2:n.420+6187T=
ENST00000475239.5:n.525+6187T=
ENST00000488550.5:c.965+6187T=	ENSP00000475161.1:n.965+6187T=
ENST00000495021.6:c.770+6187T=	ENSP00000440571.1:n.770+6187T=
ENST00000542964.5:n.398+6187T=
ENST00000560281.6:c.965+6187T=	ENSP00000454209.1:n.965+6187T=
ENST00000606455.5:n.419+6187T=
NM_002398.2:c.965+6187T=	NP_002389.1:n.965+6187T=
XM_005264321.1:c.1013+6187T=	XP_005264378.1:n.1013+6187T=
XM_005264322.1:c.965+6187T=	XP_005264379.1:n.965+6187T=
XM_005264323.1:c.1013+6187T=	XP_005264380.1:n.1013+6187T=
XM_005264324.3:c.770+6187T=	XP_005264381.1:n.770+6187T=
XM_005264325.3:c.770+6187T=	XP_005264382.1:n.770+6187T=
XR_244932.1:n.1599+6187T=
XR_244933.1:n.1599+6187T=
NM_002398.3:c.965+6187T= MANE Select	NP_002389.1:n.965+6187T=