Canonical Allele Identifier: CA2465380858
Gene: MTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150641400G= , CM000685.2:g.150641400G= GRCh38
NC_000023.10:g.149809873G= , CM000685.1:g.149809873G= GRCh37
NC_000023.9:g.149560531G= NCBI36
NG_008199.1:g.77827G= , LRG_839:g.77827G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684910.1:c.*193G= ENSP00000509844.1:n.*193G=
ENST00000685439.1:c.315G= ENSP00000508454.1:p.Arg105=
ENST00000685944.1:c.660G= ENSP00000509266.1:p.Arg220=
ENST00000686212.1:n.262G=
ENST00000687215.1:c.*415G= ENSP00000509706.1:n.*415G=
ENST00000688152.1:c.*104G= ENSP00000509360.1:n.*104G=
ENST00000688403.1:c.-85G= ENSP00000508944.1:n.-85G=
ENST00000689314.1:c.705G= ENSP00000510607.1:p.Arg235=
ENST00000689694.1:c.660G= ENSP00000508718.1:p.Arg220=
ENST00000689810.1:c.*309G= ENSP00000510635.1:n.*309G=
ENST00000690282.1:c.-85G= ENSP00000509809.1:n.-85G=
ENST00000690351.1:c.*312G= ENSP00000509728.1:n.*312G=
ENST00000691232.1:c.315G= ENSP00000509675.1:p.Arg105=
ENST00000691482.1:n.1675G=
ENST00000691686.1:c.660G= ENSP00000509784.1:p.Arg220=
ENST00000691851.1:c.660G= ENSP00000510106.1:p.Arg220=
ENST00000692015.1:c.447G= ENSP00000510634.1:p.Arg149=
ENST00000692638.1:c.*465G= ENSP00000509412.1:n.*465G=
ENST00000692852.1:c.660G= ENSP00000510337.1:p.Arg220=
ENST00000692915.1:c.*867G= ENSP00000508547.1:n.*867G=
ENST00000370396.7:c.660G= MANE Select ENSP00000359423.3:p.Arg220=
ENST00000306167.11:n.527G=
ENST00000370396.6:c.660G= ENSP00000359423.2:p.Arg220=
ENST00000490530.1:n.599G=
NM_000252.2:c.660G= , LRG_839t1:c.660G= NP_000243.1:p.Arg220=
XM_005274687.2:c.660G= XP_005274744.1:p.Arg220=
XM_011531170.1:c.726G= XP_011529472.1:p.Arg242=
XM_011531171.1:c.705G= XP_011529473.1:p.Arg235=
XM_011531172.1:c.705G= XP_011529474.1:p.Arg235=
XM_011531173.1:c.660G= XP_011529475.1:p.Arg220=
XM_011531173.2:c.660G= XP_011529475.1:p.Arg220=
XM_017029547.1:c.705G= XP_016885036.1:p.Arg235=
XM_017029548.1:c.705G= XP_016885037.1:p.Arg235=
XM_017029549.1:c.660G= XP_016885038.1:p.Arg220=
XM_017029550.1:c.549G= XP_016885039.1:p.Arg183=
XM_017029551.2:c.-85G= XP_016885040.1:n.-85G=
NM_000252.3:c.660G= MANE Select NP_000243.1:p.Arg220=
NM_001376906.1:c.660G= NP_001363835.1:p.Arg220=
NM_001376907.1:c.549G= NP_001363836.1:p.Arg183=
NM_001376908.1:c.660G= NP_001363837.1:p.Arg220=