Canonical Allele Identifier: CA1139980528

Gene: MIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222630704G= , CM000663.2:g.222630704G=	GRCh38
NC_000001.10:g.222804046G= , CM000663.1:g.222804046G=	GRCh37
NC_000001.9:g.220870669G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344922.10:c.3169+315G= MANE Select	ENSP00000340900.5:n.3169+315G=
ENST00000344507.1:c.1474+2010G=	ENSP00000341348.1:n.1474+2010G=
ENST00000344922.9:c.3169+315G=	ENSP00000340900.5:n.3169+315G=
ENST00000354906.7:c.1916+315G=
ENST00000470521.1:n.3181+315G=
NM_198551.3:c.3169+315G=	NP_940953.2:n.3169+315G=
XM_005273121.3:c.3169+315G=	XP_005273178.1:n.3169+315G=
XM_006711304.2:c.3169+315G=	XP_006711367.1:n.3169+315G=
XM_011509513.1:c.3169+315G=	XP_011507815.1:n.3169+315G=
NM_001324062.1:c.3169+315G=	NP_001310991.1:n.3169+315G=
NM_001324063.1:c.3169+315G=	NP_001310992.1:n.3169+315G=
NM_001324064.1:c.2677+315G=	NP_001310993.1:n.2677+315G=
XM_006711304.4:c.3169+315G=	XP_006711367.3:n.3169+315G=
XM_011509513.3:c.3169+315G=	XP_011507815.3:n.3169+315G=
XM_017001243.2:c.2677+315G=	XP_016856732.1:n.2677+315G=
NM_198551.4:c.3169+315G= MANE Select	NP_940953.2:n.3169+315G=
NM_001324062.2:c.3169+315G=	NP_001310991.1:n.3169+315G=
NM_001324063.2:c.3169+315G=	NP_001310992.1:n.3169+315G=
NM_001324064.2:c.2677+315G=	NP_001310993.1:n.2677+315G=