Canonical Allele Identifier: CA1143439859

Gene: MIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222658802C= , CM000663.2:g.222658802C=	GRCh38
NC_000001.10:g.222832144C= , CM000663.1:g.222832144C=	GRCh37
NC_000001.9:g.220898767C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344922.10:c.4688C= MANE Select	ENSP00000340900.5:p.Ala1563=
ENST00000340535.11:c.1322C=	ENSP00000345866.7:p.Ala441=
ENST00000344507.1:c.1475-6797C=	ENSP00000341348.1:n.1475-6797C=
ENST00000344922.9:c.4688C=	ENSP00000340900.5:p.Ala1563=
ENST00000476400.1:n.161C=
NM_001300867.1:c.1322C=	NP_001287796.1:p.Ala441=
NM_198551.3:c.4688C=	NP_940953.2:p.Ala1563=
XM_005273121.3:c.4688C=	XP_005273178.1:p.Ala1563=
XM_006711304.2:c.4511C=	XP_006711367.1:p.Ala1504=
NM_001324062.1:c.4688C=	NP_001310991.1:p.Ala1563=
NM_001324063.1:c.4511C=	NP_001310992.1:p.Ala1504=
NM_001324064.1:c.4196C=	NP_001310993.1:p.Ala1399=
NM_001324065.1:c.1322C=	NP_001310994.1:p.Ala441=
XM_006711304.4:c.4511C=	XP_006711367.3:p.Ala1504=
XM_017001243.2:c.4196C=	XP_016856732.1:p.Ala1399=
NM_198551.4:c.4688C= MANE Select	NP_940953.2:p.Ala1563=
NM_001300867.2:c.1322C=	NP_001287796.1:p.Ala441=
NM_001324062.2:c.4688C=	NP_001310991.1:p.Ala1563=
NM_001324063.2:c.4511C=	NP_001310992.1:p.Ala1504=
NM_001324064.2:c.4196C=	NP_001310993.1:p.Ala1399=
NM_001324065.2:c.1322C=	NP_001310994.1:p.Ala441=