Canonical Allele Identifier: CA2465385860
Gene: MTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150657980A= , CM000685.2:g.150657980A= GRCh38
NC_000023.10:g.149826453A= , CM000685.1:g.149826453A= GRCh37
NC_000023.9:g.149577111A= NCBI36
NG_008199.1:g.94407A= , LRG_839:g.94407A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684910.1:c.*746A= ENSP00000509844.1:n.*746A=
ENST00000685439.1:c.868A= ENSP00000508454.1:p.Ile290=
ENST00000685944.1:c.1213A= ENSP00000509266.1:p.Ile405=
ENST00000686212.1:n.815A=
ENST00000687215.1:c.*968A= ENSP00000509706.1:n.*968A=
ENST00000688152.1:c.*657A= ENSP00000509360.1:n.*657A=
ENST00000688403.1:c.469A= ENSP00000508944.1:p.Ile157=
ENST00000689314.1:c.1258A= ENSP00000510607.1:p.Ile420=
ENST00000689694.1:c.1213A= ENSP00000508718.1:p.Ile405=
ENST00000689810.1:c.*862A= ENSP00000510635.1:n.*862A=
ENST00000690282.1:c.469A= ENSP00000509809.1:p.Ile157=
ENST00000690351.1:c.*865A= ENSP00000509728.1:n.*865A=
ENST00000691232.1:c.868A= ENSP00000509675.1:p.Ile290=
ENST00000691482.1:n.2228A=
ENST00000691686.1:c.1213A= ENSP00000509784.1:p.Ile405=
ENST00000691851.1:c.1053+8079A= ENSP00000510106.1:n.1053+8079A=
ENST00000692015.1:c.1000A= ENSP00000510634.1:p.Ile334=
ENST00000692638.1:c.*1018A= ENSP00000509412.1:n.*1018A=
ENST00000692852.1:c.1024A= ENSP00000510337.1:p.Ile342=
ENST00000692915.1:c.*1359A= ENSP00000508547.1:n.*1359A=
ENST00000370396.7:c.1213A= MANE Select ENSP00000359423.3:p.Ile405=
ENST00000306167.11:n.1080A=
ENST00000370396.6:c.1213A= ENSP00000359423.2:p.Ile405=
NM_000252.2:c.1213A= , LRG_839t1:c.1213A= NP_000243.1:p.Ile405=
XM_005274687.2:c.1213A= XP_005274744.1:p.Ile405=
XM_011531170.1:c.1279A= XP_011529472.1:p.Ile427=
XM_011531171.1:c.1258A= XP_011529473.1:p.Ile420=
XM_011531172.1:c.1258A= XP_011529474.1:p.Ile420=
XM_011531173.1:c.1213A= XP_011529475.1:p.Ile405=
XM_011531173.2:c.1213A= XP_011529475.1:p.Ile405=
XM_017029547.1:c.1258A= XP_016885036.1:p.Ile420=
XM_017029548.1:c.1258A= XP_016885037.1:p.Ile420=
XM_017029549.1:c.1213A= XP_016885038.1:p.Ile405=
XM_017029550.1:c.1102A= XP_016885039.1:p.Ile368=
XM_017029551.2:c.469A= XP_016885040.1:p.Ile157=
NM_000252.3:c.1213A= MANE Select NP_000243.1:p.Ile405=
NM_001376906.1:c.1213A= NP_001363835.1:p.Ile405=
NM_001376907.1:c.1102A= NP_001363836.1:p.Ile368=
NM_001376908.1:c.1213A= NP_001363837.1:p.Ile405=