Canonical Allele Identifier: CA771419776
Gene: MEIS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.66544868T>A , CM000664.2:g.66544868T>A GRCh38
NC_000002.11:g.66772000T>A , CM000664.1:g.66772000T>A GRCh37
NC_000002.10:g.66625504T>A NCBI36
NG_011467.1:g.114469T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272369.14:c.889-3075T>A MANE Select ENSP00000272369.8:n.889-3075T>A
ENST00000272369.13:c.889-3075T>A ENSP00000272369.8:n.889-3075T>A
ENST00000398506.6:c.883-3075T>A ENSP00000381518.2:n.883-3075T>A
ENST00000409517.5:n.203-3075T>A
ENST00000450027.2:n.344-3075T>A
ENST00000475239.5:n.449-3075T>A
ENST00000488550.5:c.889-3075T>A ENSP00000475161.1:n.889-3075T>A
ENST00000495021.6:c.694-3075T>A ENSP00000440571.1:n.694-3075T>A
ENST00000542964.5:n.322-3075T>A
ENST00000560281.6:c.889-3075T>A ENSP00000454209.1:n.889-3075T>A
ENST00000606455.5:n.343-3075T>A
NM_002398.2:c.889-3075T>A NP_002389.1:n.889-3075T>A
XM_005264321.1:c.937-3075T>A XP_005264378.1:n.937-3075T>A
XM_005264322.1:c.889-3075T>A XP_005264379.1:n.889-3075T>A
XM_005264323.1:c.937-3075T>A XP_005264380.1:n.937-3075T>A
XM_005264324.3:c.694-3075T>A XP_005264381.1:n.694-3075T>A
XM_005264325.3:c.694-3075T>A XP_005264382.1:n.694-3075T>A
XR_244932.1:n.1523-3075T>A
XR_244933.1:n.1523-3075T>A
NM_002398.3:c.889-3075T>A MANE Select NP_002389.1:n.889-3075T>A
Search 100 bp 5'
Search 100 bp 3'