Canonical Allele Identifier: CA519114328

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149826386T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150657913T>A , CM000685.2:g.150657913T>A	GRCh38
NC_000023.10:g.149826386T>A , CM000685.1:g.149826386T>A	GRCh37
NC_000023.9:g.149577044T>A	NCBI36
NG_008199.1:g.94340T>A , LRG_839:g.94340T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*679T>A	ENSP00000509844.1:n.*679T>A
ENST00000685439.1:c.801T>A	ENSP00000508454.1:p.Thr267=
ENST00000685944.1:c.1146T>A	ENSP00000509266.1:p.Thr382=
ENST00000686212.1:n.748T>A
ENST00000687215.1:c.*901T>A	ENSP00000509706.1:n.*901T>A
ENST00000688152.1:c.*590T>A	ENSP00000509360.1:n.*590T>A
ENST00000688403.1:c.402T>A	ENSP00000508944.1:p.Thr134=
ENST00000689314.1:c.1191T>A	ENSP00000510607.1:p.Thr397=
ENST00000689694.1:c.1146T>A	ENSP00000508718.1:p.Thr382=
ENST00000689810.1:c.*795T>A	ENSP00000510635.1:n.*795T>A
ENST00000690282.1:c.402T>A	ENSP00000509809.1:p.Thr134=
ENST00000690351.1:c.*798T>A	ENSP00000509728.1:n.*798T>A
ENST00000691232.1:c.801T>A	ENSP00000509675.1:p.Thr267=
ENST00000691482.1:n.2161T>A
ENST00000691686.1:c.1146T>A	ENSP00000509784.1:p.Thr382=
ENST00000691851.1:c.1053+8012T>A	ENSP00000510106.1:n.1053+8012T>A
ENST00000692015.1:c.933T>A	ENSP00000510634.1:p.Thr311=
ENST00000692638.1:c.*951T>A	ENSP00000509412.1:n.*951T>A
ENST00000692852.1:c.957T>A	ENSP00000510337.1:p.Thr319=
ENST00000692915.1:c.*1292T>A	ENSP00000508547.1:n.*1292T>A
ENST00000370396.7:c.1146T>A MANE Select	ENSP00000359423.3:p.Thr382=
ENST00000306167.11:n.1013T>A
ENST00000370396.6:c.1146T>A	ENSP00000359423.2:p.Thr382=
NM_000252.2:c.1146T>A , LRG_839t1:c.1146T>A	NP_000243.1:p.Thr382=
XM_005274687.2:c.1146T>A	XP_005274744.1:p.Thr382=
XM_011531170.1:c.1212T>A	XP_011529472.1:p.Thr404=
XM_011531171.1:c.1191T>A	XP_011529473.1:p.Thr397=
XM_011531172.1:c.1191T>A	XP_011529474.1:p.Thr397=
XM_011531173.1:c.1146T>A	XP_011529475.1:p.Thr382=
XM_011531173.2:c.1146T>A	XP_011529475.1:p.Thr382=
XM_017029547.1:c.1191T>A	XP_016885036.1:p.Thr397=
XM_017029548.1:c.1191T>A	XP_016885037.1:p.Thr397=
XM_017029549.1:c.1146T>A	XP_016885038.1:p.Thr382=
XM_017029550.1:c.1035T>A	XP_016885039.1:p.Thr345=
XM_017029551.2:c.402T>A	XP_016885040.1:p.Thr134=
NM_000252.3:c.1146T>A MANE Select	NP_000243.1:p.Thr382=
NM_001376906.1:c.1146T>A	NP_001363835.1:p.Thr382=
NM_001376907.1:c.1035T>A	NP_001363836.1:p.Thr345=
NM_001376908.1:c.1146T>A	NP_001363837.1:p.Thr382=