Canonical Allele Identifier: CA771366477

Gene: MEIS1

Linked Data

• dbSNP Id: rs1234644067
• MyVariant Identifiers: chr2:g.66758500_66758501del (hg19) ; chr2:g.66531368_66531369del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66531368_66531369del , CM000664.2:g.66531368_66531369del	GRCh38
NC_000002.11:g.66758500_66758501del , CM000664.1:g.66758500_66758501del	GRCh37
NC_000002.10:g.66612004_66612005del	NCBI36
NG_011467.1:g.100969_100970del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272369.14:c.889-16575_889-16574del MANE Select	ENSP00000272369.8:n.889-16575_889-16574del
ENST00000272369.13:c.889-16575_889-16574del	ENSP00000272369.8:n.889-16575_889-16574del
ENST00000398506.6:c.883-16575_883-16574del	ENSP00000381518.2:n.883-16575_883-16574del
ENST00000409517.5:n.203-16575_203-16574del
ENST00000450027.2:n.344-16575_344-16574del
ENST00000475239.5:n.449-16575_449-16574del
ENST00000488550.5:c.889-16575_889-16574del	ENSP00000475161.1:n.889-16575_889-16574del
ENST00000495021.6:c.694-16575_694-16574del	ENSP00000440571.1:n.694-16575_694-16574del
ENST00000542964.5:n.322-16575_322-16574del
ENST00000560281.6:c.889-16575_889-16574del	ENSP00000454209.1:n.889-16575_889-16574del
ENST00000606455.5:n.343-16575_343-16574del
NM_002398.2:c.889-16575_889-16574del	NP_002389.1:n.889-16575_889-16574del
XM_005264321.1:c.937-16575_937-16574del	XP_005264378.1:n.937-16575_937-16574del
XM_005264322.1:c.889-16575_889-16574del	XP_005264379.1:n.889-16575_889-16574del
XM_005264323.1:c.937-16575_937-16574del	XP_005264380.1:n.937-16575_937-16574del
XM_005264324.3:c.694-16575_694-16574del	XP_005264381.1:n.694-16575_694-16574del
XM_005264325.3:c.694-16575_694-16574del	XP_005264382.1:n.694-16575_694-16574del
XR_244932.1:n.1523-16575_1523-16574del
XR_244933.1:n.1523-16575_1523-16574del
NM_002398.3:c.889-16575_889-16574del MANE Select	NP_002389.1:n.889-16575_889-16574del