Canonical Allele Identifier: CA423455635

Gene: MIA3

Linked Data

• MyVariant Identifiers: chr1:g.222832139G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222658797G>T , CM000663.2:g.222658797G>T	GRCh38
NC_000001.10:g.222832139G>T , CM000663.1:g.222832139G>T	GRCh37
NC_000001.9:g.220898762G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344922.10:c.4683G>T MANE Select	ENSP00000340900.5:p.Ser1561=
ENST00000340535.11:c.1317G>T	ENSP00000345866.7:p.Ser439=
ENST00000344507.1:c.1475-6802G>T	ENSP00000341348.1:n.1475-6802G>T
ENST00000344922.9:c.4683G>T	ENSP00000340900.5:p.Ser1561=
ENST00000476400.1:n.156G>T
NM_001300867.1:c.1317G>T	NP_001287796.1:p.Ser439=
NM_198551.3:c.4683G>T	NP_940953.2:p.Ser1561=
XM_005273121.3:c.4683G>T	XP_005273178.1:p.Ser1561=
XM_006711304.2:c.4506G>T	XP_006711367.1:p.Ser1502=
NM_001324062.1:c.4683G>T	NP_001310991.1:p.Ser1561=
NM_001324063.1:c.4506G>T	NP_001310992.1:p.Ser1502=
NM_001324064.1:c.4191G>T	NP_001310993.1:p.Ser1397=
NM_001324065.1:c.1317G>T	NP_001310994.1:p.Ser439=
XM_006711304.4:c.4506G>T	XP_006711367.3:p.Ser1502=
XM_017001243.2:c.4191G>T	XP_016856732.1:p.Ser1397=
NM_198551.4:c.4683G>T MANE Select	NP_940953.2:p.Ser1561=
NM_001300867.2:c.1317G>T	NP_001287796.1:p.Ser439=
NM_001324062.2:c.4683G>T	NP_001310991.1:p.Ser1561=
NM_001324063.2:c.4506G>T	NP_001310992.1:p.Ser1502=
NM_001324064.2:c.4191G>T	NP_001310993.1:p.Ser1397=
NM_001324065.2:c.1317G>T	NP_001310994.1:p.Ser439=