Canonical Allele Identifier: CA344672932

Gene: MIA3

Linked Data

• MyVariant Identifiers: chr1:g.222832148G>C (hg19) ; chr1:g.222658806G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222658806G>C , CM000663.2:g.222658806G>C	GRCh38
NC_000001.10:g.222832148G>C , CM000663.1:g.222832148G>C	GRCh37
NC_000001.9:g.220898771G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344922.10:c.4692G>C MANE Select	ENSP00000340900.5:p.Glu1564Asp
ENST00000340535.11:c.1326G>C	ENSP00000345866.7:p.Glu442Asp
ENST00000344507.1:c.1475-6793G>C	ENSP00000341348.1:n.1475-6793G>C
ENST00000344922.9:c.4692G>C	ENSP00000340900.5:p.Glu1564Asp
ENST00000476400.1:n.165G>C
NM_001300867.1:c.1326G>C	NP_001287796.1:p.Glu442Asp
NM_198551.3:c.4692G>C	NP_940953.2:p.Glu1564Asp
XM_005273121.3:c.4692G>C	XP_005273178.1:p.Glu1564Asp
XM_006711304.2:c.4515G>C	XP_006711367.1:p.Glu1505Asp
NM_001324062.1:c.4692G>C	NP_001310991.1:p.Glu1564Asp
NM_001324063.1:c.4515G>C	NP_001310992.1:p.Glu1505Asp
NM_001324064.1:c.4200G>C	NP_001310993.1:p.Glu1400Asp
NM_001324065.1:c.1326G>C	NP_001310994.1:p.Glu442Asp
XM_006711304.4:c.4515G>C	XP_006711367.3:p.Glu1505Asp
XM_017001243.2:c.4200G>C	XP_016856732.1:p.Glu1400Asp
NM_198551.4:c.4692G>C MANE Select	NP_940953.2:p.Glu1564Asp
NM_001300867.2:c.1326G>C	NP_001287796.1:p.Glu442Asp
NM_001324062.2:c.4692G>C	NP_001310991.1:p.Glu1564Asp
NM_001324063.2:c.4515G>C	NP_001310992.1:p.Glu1505Asp
NM_001324064.2:c.4200G>C	NP_001310993.1:p.Glu1400Asp
NM_001324065.2:c.1326G>C	NP_001310994.1:p.Glu442Asp