Canonical Allele Identifier: CA533571944

Gene: MEIS1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66522885T>A , CM000664.2:g.66522885T>A	GRCh38
NC_000002.11:g.66750017T>A , CM000664.1:g.66750017T>A	GRCh37
NC_000002.10:g.66603521T>A	NCBI36
NG_011467.1:g.92486T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272369.14:c.888+10591T>A MANE Select	ENSP00000272369.8:n.888+10591T>A
ENST00000272369.13:c.888+10591T>A	ENSP00000272369.8:n.888+10591T>A
ENST00000398506.6:c.882+10591T>A	ENSP00000381518.2:n.882+10591T>A
ENST00000409517.5:n.203-25058T>A
ENST00000450027.2:n.343+10591T>A
ENST00000475239.5:n.448+10591T>A
ENST00000488550.5:c.888+10591T>A	ENSP00000475161.1:n.888+10591T>A
ENST00000495021.6:c.693+10591T>A	ENSP00000440571.1:n.693+10591T>A
ENST00000542964.5:n.321+10591T>A
ENST00000560281.6:c.888+10591T>A	ENSP00000454209.1:n.888+10591T>A
ENST00000606455.5:n.342+10591T>A
NM_002398.2:c.888+10591T>A	NP_002389.1:n.888+10591T>A
XM_005264321.1:c.936+10591T>A	XP_005264378.1:n.936+10591T>A
XM_005264322.1:c.888+10591T>A	XP_005264379.1:n.888+10591T>A
XM_005264323.1:c.936+10591T>A	XP_005264380.1:n.936+10591T>A
XM_005264324.3:c.693+10591T>A	XP_005264381.1:n.693+10591T>A
XM_005264325.3:c.693+10591T>A	XP_005264382.1:n.693+10591T>A
XR_244932.1:n.1523-25058T>A
XR_244933.1:n.1523-25058T>A
NM_002398.3:c.888+10591T>A MANE Select	NP_002389.1:n.888+10591T>A