Canonical Allele Identifier: CA2465380833
Gene: MTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150641320C= , CM000685.2:g.150641320C= GRCh38
NC_000023.10:g.149809793C= , CM000685.1:g.149809793C= GRCh37
NC_000023.9:g.149560451C= NCBI36
NG_008199.1:g.77747C= , LRG_839:g.77747C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684910.1:c.*113C= ENSP00000509844.1:n.*113C=
ENST00000685439.1:c.235C= ENSP00000508454.1:p.Leu79=
ENST00000685944.1:c.580C= ENSP00000509266.1:p.Leu194=
ENST00000686212.1:n.182C=
ENST00000687215.1:c.*335C= ENSP00000509706.1:n.*335C=
ENST00000688152.1:c.*24C= ENSP00000509360.1:n.*24C=
ENST00000688403.1:c.-165C= ENSP00000508944.1:n.-165C=
ENST00000689314.1:c.625C= ENSP00000510607.1:p.Leu209=
ENST00000689694.1:c.580C= ENSP00000508718.1:p.Leu194=
ENST00000689810.1:c.*229C= ENSP00000510635.1:n.*229C=
ENST00000690282.1:c.-165C= ENSP00000509809.1:n.-165C=
ENST00000690351.1:c.*232C= ENSP00000509728.1:n.*232C=
ENST00000691232.1:c.235C= ENSP00000509675.1:p.Leu79=
ENST00000691482.1:n.1595C=
ENST00000691686.1:c.580C= ENSP00000509784.1:p.Leu194=
ENST00000691851.1:c.580C= ENSP00000510106.1:p.Leu194=
ENST00000692015.1:c.367C= ENSP00000510634.1:p.Leu123=
ENST00000692638.1:c.*385C= ENSP00000509412.1:n.*385C=
ENST00000692852.1:c.580C= ENSP00000510337.1:p.Leu194=
ENST00000692915.1:c.*787C= ENSP00000508547.1:n.*787C=
ENST00000370396.7:c.580C= MANE Select ENSP00000359423.3:p.Leu194=
ENST00000306167.11:n.447C=
ENST00000370396.6:c.580C= ENSP00000359423.2:p.Leu194=
ENST00000490530.1:n.519C=
NM_000252.2:c.580C= , LRG_839t1:c.580C= NP_000243.1:p.Leu194=
XM_005274687.2:c.580C= XP_005274744.1:p.Leu194=
XM_011531170.1:c.646C= XP_011529472.1:p.Leu216=
XM_011531171.1:c.625C= XP_011529473.1:p.Leu209=
XM_011531172.1:c.625C= XP_011529474.1:p.Leu209=
XM_011531173.1:c.580C= XP_011529475.1:p.Leu194=
XM_011531173.2:c.580C= XP_011529475.1:p.Leu194=
XM_017029547.1:c.625C= XP_016885036.1:p.Leu209=
XM_017029548.1:c.625C= XP_016885037.1:p.Leu209=
XM_017029549.1:c.580C= XP_016885038.1:p.Leu194=
XM_017029550.1:c.469C= XP_016885039.1:p.Leu157=
XM_017029551.2:c.-165C= XP_016885040.1:n.-165C=
NM_000252.3:c.580C= MANE Select NP_000243.1:p.Leu194=
NM_001376906.1:c.580C= NP_001363835.1:p.Leu194=
NM_001376907.1:c.469C= NP_001363836.1:p.Leu157=
NM_001376908.1:c.580C= NP_001363837.1:p.Leu194=