Canonical Allele Identifier: CA1223332768

Gene: MIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222650146C= , CM000663.2:g.222650146C=	GRCh38
NC_000001.10:g.222823488C= , CM000663.1:g.222823488C=	GRCh37
NC_000001.9:g.220890111C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000344922.10:c.3632-146C= MANE Select	ENSP00000340900.5:n.3632-146C=
ENST00000340535.11:c.266-146C=	ENSP00000345866.7:n.266-146C=
ENST00000344507.1:c.1475-15453C=	ENSP00000341348.1:n.1475-15453C=
ENST00000344922.9:c.3632-146C=	ENSP00000340900.5:n.3632-146C=
ENST00000354906.7:c.2379-146C=
ENST00000467190.1:n.530-146C=
ENST00000495210.1:n.326-146C=
NM_001300867.1:c.266-146C=	NP_001287796.1:n.266-146C=
NM_198551.3:c.3632-146C=	NP_940953.2:n.3632-146C=
XM_005273121.3:c.3632-146C=	XP_005273178.1:n.3632-146C=
XM_006711304.2:c.3632-146C=	XP_006711367.1:n.3632-146C=
XM_011509513.1:c.3632-146C=	XP_011507815.1:n.3632-146C=
NM_001324062.1:c.3632-146C=	NP_001310991.1:n.3632-146C=
NM_001324063.1:c.3632-146C=	NP_001310992.1:n.3632-146C=
NM_001324064.1:c.3140-146C=	NP_001310993.1:n.3140-146C=
NM_001324065.1:c.266-146C=	NP_001310994.1:n.266-146C=
XM_006711304.4:c.3632-146C=	XP_006711367.3:n.3632-146C=
XM_011509513.3:c.3632-146C=	XP_011507815.3:n.3632-146C=
XM_017001243.2:c.3140-146C=	XP_016856732.1:n.3140-146C=
NM_198551.4:c.3632-146C= MANE Select	NP_940953.2:n.3632-146C=
NM_001300867.2:c.266-146C=	NP_001287796.1:n.266-146C=
NM_001324062.2:c.3632-146C=	NP_001310991.1:n.3632-146C=
NM_001324063.2:c.3632-146C=	NP_001310992.1:n.3632-146C=
NM_001324064.2:c.3140-146C=	NP_001310993.1:n.3140-146C=
NM_001324065.2:c.266-146C=	NP_001310994.1:n.266-146C=