Canonical Allele Identifier: CA1012663474
Gene: MIA3 HGNC NCBI

Linked Data

dbSNP Id: rs1663341632

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.222650032A>T , CM000663.2:g.222650032A>T GRCh38
NC_000001.10:g.222823374A>T , CM000663.1:g.222823374A>T GRCh37
NC_000001.9:g.220889997A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344922.10:c.3632-260A>T MANE Select ENSP00000340900.5:n.3632-260A>T
ENST00000340535.11:c.266-260A>T ENSP00000345866.7:n.266-260A>T
ENST00000344507.1:c.1475-15567A>T ENSP00000341348.1:n.1475-15567A>T
ENST00000344922.9:c.3632-260A>T ENSP00000340900.5:n.3632-260A>T
ENST00000354906.7:c.2379-260A>T
ENST00000467190.1:n.529+241A>T
ENST00000495210.1:n.326-260A>T
NM_001300867.1:c.266-260A>T NP_001287796.1:n.266-260A>T
NM_198551.3:c.3632-260A>T NP_940953.2:n.3632-260A>T
XM_005273121.3:c.3632-260A>T XP_005273178.1:n.3632-260A>T
XM_006711304.2:c.3632-260A>T XP_006711367.1:n.3632-260A>T
XM_011509513.1:c.3632-260A>T XP_011507815.1:n.3632-260A>T
NM_001324062.1:c.3632-260A>T NP_001310991.1:n.3632-260A>T
NM_001324063.1:c.3632-260A>T NP_001310992.1:n.3632-260A>T
NM_001324064.1:c.3140-260A>T NP_001310993.1:n.3140-260A>T
NM_001324065.1:c.266-260A>T NP_001310994.1:n.266-260A>T
XM_006711304.4:c.3632-260A>T XP_006711367.3:n.3632-260A>T
XM_011509513.3:c.3632-260A>T XP_011507815.3:n.3632-260A>T
XM_017001243.2:c.3140-260A>T XP_016856732.1:n.3140-260A>T
NM_198551.4:c.3632-260A>T MANE Select NP_940953.2:n.3632-260A>T
NM_001300867.2:c.266-260A>T NP_001287796.1:n.266-260A>T
NM_001324062.2:c.3632-260A>T NP_001310991.1:n.3632-260A>T
NM_001324063.2:c.3632-260A>T NP_001310992.1:n.3632-260A>T
NM_001324064.2:c.3140-260A>T NP_001310993.1:n.3140-260A>T
NM_001324065.2:c.266-260A>T NP_001310994.1:n.266-260A>T