Canonical Allele Identifier: CA2465382051
Gene: MTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150645706A= , CM000685.2:g.150645706A= GRCh38
NC_000023.10:g.149814179A= , CM000685.1:g.149814179A= GRCh37
NC_000023.9:g.149564837A= NCBI36
NG_008199.1:g.82133A= , LRG_839:g.82133A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684910.1:c.*235A= ENSP00000509844.1:n.*235A=
ENST00000685439.1:c.357A= ENSP00000508454.1:p.Glu119=
ENST00000685944.1:c.702A= ENSP00000509266.1:p.Glu234=
ENST00000686212.1:n.304A=
ENST00000687215.1:c.*457A= ENSP00000509706.1:n.*457A=
ENST00000688152.1:c.*146A= ENSP00000509360.1:n.*146A=
ENST00000688403.1:c.-43A= ENSP00000508944.1:n.-43A=
ENST00000689314.1:c.747A= ENSP00000510607.1:p.Glu249=
ENST00000689694.1:c.702A= ENSP00000508718.1:p.Glu234=
ENST00000689810.1:c.*351A= ENSP00000510635.1:n.*351A=
ENST00000690282.1:c.-43A= ENSP00000509809.1:n.-43A=
ENST00000690351.1:c.*354A= ENSP00000509728.1:n.*354A=
ENST00000691232.1:c.357A= ENSP00000509675.1:p.Glu119=
ENST00000691482.1:n.1717A=
ENST00000691686.1:c.702A= ENSP00000509784.1:p.Glu234=
ENST00000691851.1:c.702A= ENSP00000510106.1:p.Glu234=
ENST00000692015.1:c.489A= ENSP00000510634.1:p.Glu163=
ENST00000692638.1:c.*507A= ENSP00000509412.1:n.*507A=
ENST00000692852.1:c.679-4010A= ENSP00000510337.1:n.679-4010A=
ENST00000692915.1:c.*909A= ENSP00000508547.1:n.*909A=
ENST00000370396.7:c.702A= MANE Select ENSP00000359423.3:p.Glu234=
ENST00000306167.11:n.569A=
ENST00000370396.6:c.702A= ENSP00000359423.2:p.Glu234=
ENST00000490530.1:n.641A=
NM_000252.2:c.702A= , LRG_839t1:c.702A= NP_000243.1:p.Glu234=
XM_005274687.2:c.702A= XP_005274744.1:p.Glu234=
XM_011531170.1:c.768A= XP_011529472.1:p.Glu256=
XM_011531171.1:c.747A= XP_011529473.1:p.Glu249=
XM_011531172.1:c.747A= XP_011529474.1:p.Glu249=
XM_011531173.1:c.702A= XP_011529475.1:p.Glu234=
XM_011531173.2:c.702A= XP_011529475.1:p.Glu234=
XM_017029547.1:c.747A= XP_016885036.1:p.Glu249=
XM_017029548.1:c.747A= XP_016885037.1:p.Glu249=
XM_017029549.1:c.702A= XP_016885038.1:p.Glu234=
XM_017029550.1:c.591A= XP_016885039.1:p.Glu197=
XM_017029551.2:c.-43A= XP_016885040.1:n.-43A=
NM_000252.3:c.702A= MANE Select NP_000243.1:p.Glu234=
NM_001376906.1:c.702A= NP_001363835.1:p.Glu234=
NM_001376907.1:c.591A= NP_001363836.1:p.Glu197=
NM_001376908.1:c.702A= NP_001363837.1:p.Glu234=