Canonical Allele Identifier: CA2695238603
Gene: MTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150598660_150598661delinsAACT , CM000685.2:g.150598660_150598661delinsAACT GRCh38
NC_000023.10:g.149767124_149767125delinsAACT , CM000685.1:g.149767124_149767125delinsAACT GRCh37
NC_000023.9:g.149517782_149517783delinsAACT NCBI36
NG_008199.1:g.35078_35079delinsAACT , LRG_839:g.35078_35079delinsAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000684910.1:c.136+2090_136+2091delinsAACT ENSP00000509844.1:n.136+2090_136+2091delinsAACT
ENST00000685439.1:c.-3-20378_-3-20377delinsAACT ENSP00000508454.1:n.-3-20378_-3-20377delinsAACT
ENST00000685944.1:c.205_206delinsAACT ENSP00000509266.1:p.Arg69AsnfsTer5
ENST00000687215.1:c.-81_-80delinsAACT ENSP00000509706.1:n.-81_-80delinsAACT
ENST00000687365.1:n.260_261delinsAACT
ENST00000688152.1:c.205_206delinsAACT ENSP00000509360.1:p.Arg69AsnfsTer5
ENST00000688403.1:c.-301+29798_-301+29799delinsAACT ENSP00000508944.1:n.-301+29798_-301+29799delinsAACT
ENST00000689314.1:c.205_206delinsAACT ENSP00000510607.1:p.Arg69AsnfsTer5
ENST00000689694.1:c.205_206delinsAACT ENSP00000508718.1:p.Arg69AsnfsTer5
ENST00000689810.1:c.205_206delinsAACT ENSP00000510635.1:p.Arg69AsnfsTer5
ENST00000690282.1:c.-301+29942_-301+29943delinsAACT ENSP00000509809.1:n.-301+29942_-301+29943delinsAACT
ENST00000690351.1:c.136+2090_136+2091delinsAACT ENSP00000509728.1:n.136+2090_136+2091delinsAACT
ENST00000691232.1:c.-3-20378_-3-20377delinsAACT ENSP00000509675.1:n.-3-20378_-3-20377delinsAACT
ENST00000691686.1:c.205_206delinsAACT ENSP00000509784.1:p.Arg69AsnfsTer5
ENST00000691851.1:c.205_206delinsAACT ENSP00000510106.1:p.Arg69AsnfsTer5
ENST00000692015.1:c.205_206delinsAACT ENSP00000510634.1:p.Arg69AsnfsTer5
ENST00000692638.1:c.136+2090_136+2091delinsAACT ENSP00000509412.1:n.136+2090_136+2091delinsAACT
ENST00000692852.1:c.205_206delinsAACT ENSP00000510337.1:p.Arg69AsnfsTer5
ENST00000692915.1:c.205_206delinsAACT ENSP00000508547.1:p.Arg69AsnfsTer5
ENST00000693422.1:n.266_267delinsAACT
ENST00000370396.7:c.205_206delinsAACT MANE Select ENSP00000359423.3:p.Arg69AsnfsTer5
ENST00000306167.11:n.244_245delinsAACT
ENST00000370396.6:c.205_206delinsAACT ENSP00000359423.2:p.Arg69AsnfsTer5
ENST00000424519.1:c.205_206delinsAACT ENSP00000400699.1:p.Arg69AsnfsTer5
ENST00000490530.1:n.170+2090_170+2091delinsAACT
NM_000252.2:c.205_206delinsAACT , LRG_839t1:c.205_206delinsAACT NP_000243.1:p.Arg69AsnfsTer5
XM_005274687.2:c.205_206delinsAACT XP_005274744.1:p.Arg69AsnfsTer5
XM_011531170.1:c.226_227delinsAACT XP_011529472.1:p.Arg76AsnfsTer5
XM_011531171.1:c.205_206delinsAACT XP_011529473.1:p.Arg69AsnfsTer5
XM_011531172.1:c.205_206delinsAACT XP_011529474.1:p.Arg69AsnfsTer5
XM_011531173.1:c.205_206delinsAACT XP_011529475.1:p.Arg69AsnfsTer5
XM_011531173.2:c.205_206delinsAACT XP_011529475.1:p.Arg69AsnfsTer5
XM_017029547.1:c.205_206delinsAACT XP_016885036.1:p.Arg69AsnfsTer5
XM_017029548.1:c.205_206delinsAACT XP_016885037.1:p.Arg69AsnfsTer5
XM_017029549.1:c.205_206delinsAACT XP_016885038.1:p.Arg69AsnfsTer5
XM_017029550.1:c.205_206delinsAACT XP_016885039.1:p.Arg69AsnfsTer5
NM_000252.3:c.205_206delinsAACT MANE Select NP_000243.1:p.Arg69AsnfsTer5
NM_001376906.1:c.205_206delinsAACT NP_001363835.1:p.Arg69AsnfsTer5
NM_001376907.1:c.205_206delinsAACT NP_001363836.1:p.Arg69AsnfsTer5
NM_001376908.1:c.205_206delinsAACT NP_001363837.1:p.Arg69AsnfsTer5