Canonical Allele Identifier: CA2574137918

Gene: MIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222658816dup , CM000663.2:g.222658816dup	GRCh38
NC_000001.10:g.222832158dup , CM000663.1:g.222832158dup	GRCh37
NC_000001.9:g.220898781dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344922.10:c.4702dup MANE Select	ENSP00000340900.5:p.Thr1568AsnfsTer7
ENST00000340535.11:c.1336dup	ENSP00000345866.7:p.Thr446AsnfsTer7
ENST00000344507.1:c.1475-6783dup	ENSP00000341348.1:n.1475-6783dup
ENST00000344922.9:c.4702dup	ENSP00000340900.5:p.Thr1568AsnfsTer7
ENST00000476400.1:n.175dup
NM_001300867.1:c.1336dup	NP_001287796.1:p.Thr446AsnfsTer7
NM_198551.3:c.4702dup	NP_940953.2:p.Thr1568AsnfsTer7
XM_005273121.3:c.4702dup	XP_005273178.1:p.Thr1568AsnfsTer7
XM_006711304.2:c.4525dup	XP_006711367.1:p.Thr1509AsnfsTer7
NM_001324062.1:c.4702dup	NP_001310991.1:p.Thr1568AsnfsTer7
NM_001324063.1:c.4525dup	NP_001310992.1:p.Thr1509AsnfsTer7
NM_001324064.1:c.4210dup	NP_001310993.1:p.Thr1404AsnfsTer7
NM_001324065.1:c.1336dup	NP_001310994.1:p.Thr446AsnfsTer7
XM_006711304.4:c.4525dup	XP_006711367.3:p.Thr1509AsnfsTer7
XM_017001243.2:c.4210dup	XP_016856732.1:p.Thr1404AsnfsTer7
NM_198551.4:c.4702dup MANE Select	NP_940953.2:p.Thr1568AsnfsTer7
NM_001300867.2:c.1336dup	NP_001287796.1:p.Thr446AsnfsTer7
NM_001324062.2:c.4702dup	NP_001310991.1:p.Thr1568AsnfsTer7
NM_001324063.2:c.4525dup	NP_001310992.1:p.Thr1509AsnfsTer7
NM_001324064.2:c.4210dup	NP_001310993.1:p.Thr1404AsnfsTer7
NM_001324065.2:c.1336dup	NP_001310994.1:p.Thr446AsnfsTer7