Canonical Allele Identifier: CA415256118
Gene: MTM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150641345T>A , CM000685.2:g.150641345T>A GRCh38
NC_000023.10:g.149809818T>A , CM000685.1:g.149809818T>A GRCh37
NC_000023.9:g.149560476T>A NCBI36
NG_008199.1:g.77772T>A , LRG_839:g.77772T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684910.1:c.*138T>A ENSP00000509844.1:n.*138T>A
ENST00000685439.1:c.260T>A ENSP00000508454.1:p.Leu87Ter
ENST00000685944.1:c.605T>A ENSP00000509266.1:p.Leu202Ter
ENST00000686212.1:n.207T>A
ENST00000687215.1:c.*360T>A ENSP00000509706.1:n.*360T>A
ENST00000688152.1:c.*49T>A ENSP00000509360.1:n.*49T>A
ENST00000688403.1:c.-140T>A ENSP00000508944.1:n.-140T>A
ENST00000689314.1:c.650T>A ENSP00000510607.1:p.Leu217Ter
ENST00000689694.1:c.605T>A ENSP00000508718.1:p.Leu202Ter
ENST00000689810.1:c.*254T>A ENSP00000510635.1:n.*254T>A
ENST00000690282.1:c.-140T>A ENSP00000509809.1:n.-140T>A
ENST00000690351.1:c.*257T>A ENSP00000509728.1:n.*257T>A
ENST00000691232.1:c.260T>A ENSP00000509675.1:p.Leu87Ter
ENST00000691482.1:n.1620T>A
ENST00000691686.1:c.605T>A ENSP00000509784.1:p.Leu202Ter
ENST00000691851.1:c.605T>A ENSP00000510106.1:p.Leu202Ter
ENST00000692015.1:c.392T>A ENSP00000510634.1:p.Leu131Ter
ENST00000692638.1:c.*410T>A ENSP00000509412.1:n.*410T>A
ENST00000692852.1:c.605T>A ENSP00000510337.1:p.Leu202Ter
ENST00000692915.1:c.*812T>A ENSP00000508547.1:n.*812T>A
ENST00000370396.7:c.605T>A MANE Select ENSP00000359423.3:p.Leu202Ter
ENST00000306167.11:n.472T>A
ENST00000370396.6:c.605T>A ENSP00000359423.2:p.Leu202Ter
ENST00000490530.1:n.544T>A
NM_000252.2:c.605T>A , LRG_839t1:c.605T>A NP_000243.1:p.Leu202Ter
XM_005274687.2:c.605T>A XP_005274744.1:p.Leu202Ter
XM_011531170.1:c.671T>A XP_011529472.1:p.Leu224Ter
XM_011531171.1:c.650T>A XP_011529473.1:p.Leu217Ter
XM_011531172.1:c.650T>A XP_011529474.1:p.Leu217Ter
XM_011531173.1:c.605T>A XP_011529475.1:p.Leu202Ter
XM_011531173.2:c.605T>A XP_011529475.1:p.Leu202Ter
XM_017029547.1:c.650T>A XP_016885036.1:p.Leu217Ter
XM_017029548.1:c.650T>A XP_016885037.1:p.Leu217Ter
XM_017029549.1:c.605T>A XP_016885038.1:p.Leu202Ter
XM_017029550.1:c.494T>A XP_016885039.1:p.Leu165Ter
XM_017029551.2:c.-140T>A XP_016885040.1:n.-140T>A
NM_000252.3:c.605T>A MANE Select NP_000243.1:p.Leu202Ter
NM_001376906.1:c.605T>A NP_001363835.1:p.Leu202Ter
NM_001376907.1:c.494T>A NP_001363836.1:p.Leu165Ter
NM_001376908.1:c.605T>A NP_001363837.1:p.Leu202Ter