Canonical Allele Identifier: CA519114594

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149826455A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150657982A>C , CM000685.2:g.150657982A>C	GRCh38
NC_000023.10:g.149826455A>C , CM000685.1:g.149826455A>C	GRCh37
NC_000023.9:g.149577113A>C	NCBI36
NG_008199.1:g.94409A>C , LRG_839:g.94409A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*748A>C	ENSP00000509844.1:n.*748A>C
ENST00000685439.1:c.870A>C	ENSP00000508454.1:p.Ile290=
ENST00000685944.1:c.1215A>C	ENSP00000509266.1:p.Ile405=
ENST00000686212.1:n.817A>C
ENST00000687215.1:c.*970A>C	ENSP00000509706.1:n.*970A>C
ENST00000688152.1:c.*659A>C	ENSP00000509360.1:n.*659A>C
ENST00000688403.1:c.471A>C	ENSP00000508944.1:p.Ile157=
ENST00000689314.1:c.1260A>C	ENSP00000510607.1:p.Ile420=
ENST00000689694.1:c.1215A>C	ENSP00000508718.1:p.Ile405=
ENST00000689810.1:c.*864A>C	ENSP00000510635.1:n.*864A>C
ENST00000690282.1:c.471A>C	ENSP00000509809.1:p.Ile157=
ENST00000690351.1:c.*867A>C	ENSP00000509728.1:n.*867A>C
ENST00000691232.1:c.870A>C	ENSP00000509675.1:p.Ile290=
ENST00000691482.1:n.2230A>C
ENST00000691686.1:c.1215A>C	ENSP00000509784.1:p.Ile405=
ENST00000691851.1:c.1053+8081A>C	ENSP00000510106.1:n.1053+8081A>C
ENST00000692015.1:c.1002A>C	ENSP00000510634.1:p.Ile334=
ENST00000692638.1:c.*1020A>C	ENSP00000509412.1:n.*1020A>C
ENST00000692852.1:c.1026A>C	ENSP00000510337.1:p.Ile342=
ENST00000692915.1:c.*1361A>C	ENSP00000508547.1:n.*1361A>C
ENST00000370396.7:c.1215A>C MANE Select	ENSP00000359423.3:p.Ile405=
ENST00000306167.11:n.1082A>C
ENST00000370396.6:c.1215A>C	ENSP00000359423.2:p.Ile405=
NM_000252.2:c.1215A>C , LRG_839t1:c.1215A>C	NP_000243.1:p.Ile405=
XM_005274687.2:c.1215A>C	XP_005274744.1:p.Ile405=
XM_011531170.1:c.1281A>C	XP_011529472.1:p.Ile427=
XM_011531171.1:c.1260A>C	XP_011529473.1:p.Ile420=
XM_011531172.1:c.1260A>C	XP_011529474.1:p.Ile420=
XM_011531173.1:c.1215A>C	XP_011529475.1:p.Ile405=
XM_011531173.2:c.1215A>C	XP_011529475.1:p.Ile405=
XM_017029547.1:c.1260A>C	XP_016885036.1:p.Ile420=
XM_017029548.1:c.1260A>C	XP_016885037.1:p.Ile420=
XM_017029549.1:c.1215A>C	XP_016885038.1:p.Ile405=
XM_017029550.1:c.1104A>C	XP_016885039.1:p.Ile368=
XM_017029551.2:c.471A>C	XP_016885040.1:p.Ile157=
NM_000252.3:c.1215A>C MANE Select	NP_000243.1:p.Ile405=
NM_001376906.1:c.1215A>C	NP_001363835.1:p.Ile405=
NM_001376907.1:c.1104A>C	NP_001363836.1:p.Ile368=
NM_001376908.1:c.1215A>C	NP_001363837.1:p.Ile405=