Canonical Allele Identifier: CA344672903

Gene: MIA3

Linked Data

• MyVariant Identifiers: chr1:g.222832132C>T (hg19) ; chr1:g.222658790C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222658790C>T , CM000663.2:g.222658790C>T	GRCh38
NC_000001.10:g.222832132C>T , CM000663.1:g.222832132C>T	GRCh37
NC_000001.9:g.220898755C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344922.10:c.4676C>T MANE Select	ENSP00000340900.5:p.Ala1559Val
ENST00000340535.11:c.1310C>T	ENSP00000345866.7:p.Ala437Val
ENST00000344507.1:c.1475-6809C>T	ENSP00000341348.1:n.1475-6809C>T
ENST00000344922.9:c.4676C>T	ENSP00000340900.5:p.Ala1559Val
ENST00000476400.1:n.149C>T
NM_001300867.1:c.1310C>T	NP_001287796.1:p.Ala437Val
NM_198551.3:c.4676C>T	NP_940953.2:p.Ala1559Val
XM_005273121.3:c.4676C>T	XP_005273178.1:p.Ala1559Val
XM_006711304.2:c.4499C>T	XP_006711367.1:p.Ala1500Val
NM_001324062.1:c.4676C>T	NP_001310991.1:p.Ala1559Val
NM_001324063.1:c.4499C>T	NP_001310992.1:p.Ala1500Val
NM_001324064.1:c.4184C>T	NP_001310993.1:p.Ala1395Val
NM_001324065.1:c.1310C>T	NP_001310994.1:p.Ala437Val
XM_006711304.4:c.4499C>T	XP_006711367.3:p.Ala1500Val
XM_017001243.2:c.4184C>T	XP_016856732.1:p.Ala1395Val
NM_198551.4:c.4676C>T MANE Select	NP_940953.2:p.Ala1559Val
NM_001300867.2:c.1310C>T	NP_001287796.1:p.Ala437Val
NM_001324062.2:c.4676C>T	NP_001310991.1:p.Ala1559Val
NM_001324063.2:c.4499C>T	NP_001310992.1:p.Ala1500Val
NM_001324064.2:c.4184C>T	NP_001310993.1:p.Ala1395Val
NM_001324065.2:c.1310C>T	NP_001310994.1:p.Ala437Val