Canonical Allele Identifier: CA1223337058
Gene: MIA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.222658862A= , CM000663.2:g.222658862A= GRCh38
NC_000001.10:g.222832204A= , CM000663.1:g.222832204A= GRCh37
NC_000001.9:g.220898827A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344922.10:c.4709+39A= MANE Select ENSP00000340900.5:n.4709+39A=
ENST00000340535.11:c.1343+39A= ENSP00000345866.7:n.1343+39A=
ENST00000344507.1:c.1475-6737A= ENSP00000341348.1:n.1475-6737A=
ENST00000344922.9:c.4709+39A= ENSP00000340900.5:n.4709+39A=
ENST00000476400.1:n.182+39A=
NM_001300867.1:c.1343+39A= NP_001287796.1:n.1343+39A=
NM_198551.3:c.4709+39A= NP_940953.2:n.4709+39A=
XM_005273121.3:c.4709+39A= XP_005273178.1:n.4709+39A=
XM_006711304.2:c.4532+39A= XP_006711367.1:n.4532+39A=
NM_001324062.1:c.4709+39A= NP_001310991.1:n.4709+39A=
NM_001324063.1:c.4532+39A= NP_001310992.1:n.4532+39A=
NM_001324064.1:c.4217+39A= NP_001310993.1:n.4217+39A=
NM_001324065.1:c.1343+39A= NP_001310994.1:n.1343+39A=
XM_006711304.4:c.4532+39A= XP_006711367.3:n.4532+39A=
XM_017001243.2:c.4217+39A= XP_016856732.1:n.4217+39A=
NM_198551.4:c.4709+39A= MANE Select NP_940953.2:n.4709+39A=
NM_001300867.2:c.1343+39A= NP_001287796.1:n.1343+39A=
NM_001324062.2:c.4709+39A= NP_001310991.1:n.4709+39A=
NM_001324063.2:c.4532+39A= NP_001310992.1:n.4532+39A=
NM_001324064.2:c.4217+39A= NP_001310993.1:n.4217+39A=
NM_001324065.2:c.1343+39A= NP_001310994.1:n.1343+39A=