Canonical Allele Identifier: CA344672961

Gene: MIA3

Linked Data

• MyVariant Identifiers: chr1:g.222832159C>G (hg19) ; chr1:g.222658817C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222658817C>G , CM000663.2:g.222658817C>G	GRCh38
NC_000001.10:g.222832159C>G , CM000663.1:g.222832159C>G	GRCh37
NC_000001.9:g.220898782C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344922.10:c.4703C>G MANE Select	ENSP00000340900.5:p.Thr1568Ser
ENST00000340535.11:c.1337C>G	ENSP00000345866.7:p.Thr446Ser
ENST00000344507.1:c.1475-6782C>G	ENSP00000341348.1:n.1475-6782C>G
ENST00000344922.9:c.4703C>G	ENSP00000340900.5:p.Thr1568Ser
ENST00000476400.1:n.176C>G
NM_001300867.1:c.1337C>G	NP_001287796.1:p.Thr446Ser
NM_198551.3:c.4703C>G	NP_940953.2:p.Thr1568Ser
XM_005273121.3:c.4703C>G	XP_005273178.1:p.Thr1568Ser
XM_006711304.2:c.4526C>G	XP_006711367.1:p.Thr1509Ser
NM_001324062.1:c.4703C>G	NP_001310991.1:p.Thr1568Ser
NM_001324063.1:c.4526C>G	NP_001310992.1:p.Thr1509Ser
NM_001324064.1:c.4211C>G	NP_001310993.1:p.Thr1404Ser
NM_001324065.1:c.1337C>G	NP_001310994.1:p.Thr446Ser
XM_006711304.4:c.4526C>G	XP_006711367.3:p.Thr1509Ser
XM_017001243.2:c.4211C>G	XP_016856732.1:p.Thr1404Ser
NM_198551.4:c.4703C>G MANE Select	NP_940953.2:p.Thr1568Ser
NM_001300867.2:c.1337C>G	NP_001287796.1:p.Thr446Ser
NM_001324062.2:c.4703C>G	NP_001310991.1:p.Thr1568Ser
NM_001324063.2:c.4526C>G	NP_001310992.1:p.Thr1509Ser
NM_001324064.2:c.4211C>G	NP_001310993.1:p.Thr1404Ser
NM_001324065.2:c.1337C>G	NP_001310994.1:p.Thr446Ser