Canonical Allele Identifier: CA1257745095

Gene: MEIS1

Linked Data

• dbSNP Id: rs1674382400

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66531221_66531230del , CM000664.2:g.66531221_66531230del	GRCh38
NC_000002.11:g.66758353_66758362del , CM000664.1:g.66758353_66758362del	GRCh37
NC_000002.10:g.66611857_66611866del	NCBI36
NG_011467.1:g.100822_100831del

Transcript Alleles

HGVS	Amino-acid change
ENST00000272369.14:c.889-16722_889-16713del MANE Select	ENSP00000272369.8:n.889-16722_889-16713del
ENST00000272369.13:c.889-16722_889-16713del	ENSP00000272369.8:n.889-16722_889-16713del
ENST00000398506.6:c.883-16722_883-16713del	ENSP00000381518.2:n.883-16722_883-16713del
ENST00000409517.5:n.203-16722_203-16713del
ENST00000450027.2:n.344-16722_344-16713del
ENST00000475239.5:n.449-16722_449-16713del
ENST00000488550.5:c.889-16722_889-16713del	ENSP00000475161.1:n.889-16722_889-16713del
ENST00000495021.6:c.694-16722_694-16713del	ENSP00000440571.1:n.694-16722_694-16713del
ENST00000542964.5:n.322-16722_322-16713del
ENST00000560281.6:c.889-16722_889-16713del	ENSP00000454209.1:n.889-16722_889-16713del
ENST00000606455.5:n.343-16722_343-16713del
NM_002398.2:c.889-16722_889-16713del	NP_002389.1:n.889-16722_889-16713del
XM_005264321.1:c.937-16722_937-16713del	XP_005264378.1:n.937-16722_937-16713del
XM_005264322.1:c.889-16722_889-16713del	XP_005264379.1:n.889-16722_889-16713del
XM_005264323.1:c.937-16722_937-16713del	XP_005264380.1:n.937-16722_937-16713del
XM_005264324.3:c.694-16722_694-16713del	XP_005264381.1:n.694-16722_694-16713del
XM_005264325.3:c.694-16722_694-16713del	XP_005264382.1:n.694-16722_694-16713del
XR_244932.1:n.1523-16722_1523-16713del
XR_244933.1:n.1523-16722_1523-16713del
NM_002398.3:c.889-16722_889-16713del MANE Select	NP_002389.1:n.889-16722_889-16713del