Canonical Allele Identifier: CA1257745124

Gene: MEIS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66531296C= , CM000664.2:g.66531296C=	GRCh38
NC_000002.11:g.66758428C= , CM000664.1:g.66758428C=	GRCh37
NC_000002.10:g.66611932C=	NCBI36
NG_011467.1:g.100897C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272369.14:c.889-16647C= MANE Select	ENSP00000272369.8:n.889-16647C=
ENST00000272369.13:c.889-16647C=	ENSP00000272369.8:n.889-16647C=
ENST00000398506.6:c.883-16647C=	ENSP00000381518.2:n.883-16647C=
ENST00000409517.5:n.203-16647C=
ENST00000450027.2:n.344-16647C=
ENST00000475239.5:n.449-16647C=
ENST00000488550.5:c.889-16647C=	ENSP00000475161.1:n.889-16647C=
ENST00000495021.6:c.694-16647C=	ENSP00000440571.1:n.694-16647C=
ENST00000542964.5:n.322-16647C=
ENST00000560281.6:c.889-16647C=	ENSP00000454209.1:n.889-16647C=
ENST00000606455.5:n.343-16647C=
NM_002398.2:c.889-16647C=	NP_002389.1:n.889-16647C=
XM_005264321.1:c.937-16647C=	XP_005264378.1:n.937-16647C=
XM_005264322.1:c.889-16647C=	XP_005264379.1:n.889-16647C=
XM_005264323.1:c.937-16647C=	XP_005264380.1:n.937-16647C=
XM_005264324.3:c.694-16647C=	XP_005264381.1:n.694-16647C=
XM_005264325.3:c.694-16647C=	XP_005264382.1:n.694-16647C=
XR_244932.1:n.1523-16647C=
XR_244933.1:n.1523-16647C=
NM_002398.3:c.889-16647C= MANE Select	NP_002389.1:n.889-16647C=