Canonical Allele Identifier: CA1223337154
Gene: MIA3 HGNC NCBI

Linked Data

dbSNP Id: rs1663881969

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.222659186_222659191del , CM000663.2:g.222659186_222659191del GRCh38
NC_000001.10:g.222832528_222832533del , CM000663.1:g.222832528_222832533del GRCh37
NC_000001.9:g.220899151_220899156del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000344922.10:c.4710-267_4710-262del MANE Select ENSP00000340900.5:n.4710-267_4710-262del
ENST00000340535.11:c.1344-267_1344-262del ENSP00000345866.7:n.1344-267_1344-262del
ENST00000344507.1:c.1475-6413_1475-6408del ENSP00000341348.1:n.1475-6413_1475-6408del
ENST00000344922.9:c.4710-267_4710-262del ENSP00000340900.5:n.4710-267_4710-262del
ENST00000476400.1:n.183-267_183-262del
NM_001300867.1:c.1344-267_1344-262del NP_001287796.1:n.1344-267_1344-262del
NM_198551.3:c.4710-267_4710-262del NP_940953.2:n.4710-267_4710-262del
XM_005273121.3:c.4710-267_4710-262del XP_005273178.1:n.4710-267_4710-262del
XM_006711304.2:c.4533-267_4533-262del XP_006711367.1:n.4533-267_4533-262del
NM_001324062.1:c.4710-267_4710-262del NP_001310991.1:n.4710-267_4710-262del
NM_001324063.1:c.4533-267_4533-262del NP_001310992.1:n.4533-267_4533-262del
NM_001324064.1:c.4218-267_4218-262del NP_001310993.1:n.4218-267_4218-262del
NM_001324065.1:c.1344-267_1344-262del NP_001310994.1:n.1344-267_1344-262del
XM_006711304.4:c.4533-267_4533-262del XP_006711367.3:n.4533-267_4533-262del
XM_017001243.2:c.4218-267_4218-262del XP_016856732.1:n.4218-267_4218-262del
NM_198551.4:c.4710-267_4710-262del MANE Select NP_940953.2:n.4710-267_4710-262del
NM_001300867.2:c.1344-267_1344-262del NP_001287796.1:n.1344-267_1344-262del
NM_001324062.2:c.4710-267_4710-262del NP_001310991.1:n.4710-267_4710-262del
NM_001324063.2:c.4533-267_4533-262del NP_001310992.1:n.4533-267_4533-262del
NM_001324064.2:c.4218-267_4218-262del NP_001310993.1:n.4218-267_4218-262del
NM_001324065.2:c.1344-267_1344-262del NP_001310994.1:n.1344-267_1344-262del