Canonical Allele Identifier: CA2747888626

Gene: MIA3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.222659200_222659203del , CM000663.2:g.222659200_222659203del	GRCh38
NC_000001.10:g.222832542_222832545del , CM000663.1:g.222832542_222832545del	GRCh37
NC_000001.9:g.220899165_220899168del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344922.10:c.4710-253_4710-250del MANE Select	ENSP00000340900.5:n.4710-253_4710-250del
ENST00000340535.11:c.1344-253_1344-250del	ENSP00000345866.7:n.1344-253_1344-250del
ENST00000344507.1:c.1475-6399_1475-6396del	ENSP00000341348.1:n.1475-6399_1475-6396del
ENST00000344922.9:c.4710-253_4710-250del	ENSP00000340900.5:n.4710-253_4710-250del
ENST00000476400.1:n.183-253_183-250del
NM_001300867.1:c.1344-253_1344-250del	NP_001287796.1:n.1344-253_1344-250del
NM_198551.3:c.4710-253_4710-250del	NP_940953.2:n.4710-253_4710-250del
XM_005273121.3:c.4710-253_4710-250del	XP_005273178.1:n.4710-253_4710-250del
XM_006711304.2:c.4533-253_4533-250del	XP_006711367.1:n.4533-253_4533-250del
NM_001324062.1:c.4710-253_4710-250del	NP_001310991.1:n.4710-253_4710-250del
NM_001324063.1:c.4533-253_4533-250del	NP_001310992.1:n.4533-253_4533-250del
NM_001324064.1:c.4218-253_4218-250del	NP_001310993.1:n.4218-253_4218-250del
NM_001324065.1:c.1344-253_1344-250del	NP_001310994.1:n.1344-253_1344-250del
XM_006711304.4:c.4533-253_4533-250del	XP_006711367.3:n.4533-253_4533-250del
XM_017001243.2:c.4218-253_4218-250del	XP_016856732.1:n.4218-253_4218-250del
NM_198551.4:c.4710-253_4710-250del MANE Select	NP_940953.2:n.4710-253_4710-250del
NM_001300867.2:c.1344-253_1344-250del	NP_001287796.1:n.1344-253_1344-250del
NM_001324062.2:c.4710-253_4710-250del	NP_001310991.1:n.4710-253_4710-250del
NM_001324063.2:c.4533-253_4533-250del	NP_001310992.1:n.4533-253_4533-250del
NM_001324064.2:c.4218-253_4218-250del	NP_001310993.1:n.4218-253_4218-250del
NM_001324065.2:c.1344-253_1344-250del	NP_001310994.1:n.1344-253_1344-250del