Canonical Allele Identifier: CA2465380830
Gene: MTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150641311T= , CM000685.2:g.150641311T= GRCh38
NC_000023.10:g.149809784T= , CM000685.1:g.149809784T= GRCh37
NC_000023.9:g.149560442T= NCBI36
NG_008199.1:g.77738T= , LRG_839:g.77738T=

Transcript Alleles

HGVS Amino-acid change
ENST00000684910.1:c.*104T= ENSP00000509844.1:n.*104T=
ENST00000685439.1:c.226T= ENSP00000508454.1:p.Cys76=
ENST00000685944.1:c.571T= ENSP00000509266.1:p.Cys191=
ENST00000686212.1:n.173T=
ENST00000687215.1:c.*326T= ENSP00000509706.1:n.*326T=
ENST00000688152.1:c.*15T= ENSP00000509360.1:n.*15T=
ENST00000688403.1:c.-174T= ENSP00000508944.1:n.-174T=
ENST00000689314.1:c.616T= ENSP00000510607.1:p.Cys206=
ENST00000689694.1:c.571T= ENSP00000508718.1:p.Cys191=
ENST00000689810.1:c.*220T= ENSP00000510635.1:n.*220T=
ENST00000690282.1:c.-174T= ENSP00000509809.1:n.-174T=
ENST00000690351.1:c.*223T= ENSP00000509728.1:n.*223T=
ENST00000691232.1:c.226T= ENSP00000509675.1:p.Cys76=
ENST00000691482.1:n.1586T=
ENST00000691686.1:c.571T= ENSP00000509784.1:p.Cys191=
ENST00000691851.1:c.571T= ENSP00000510106.1:p.Cys191=
ENST00000692015.1:c.358T= ENSP00000510634.1:p.Cys120=
ENST00000692638.1:c.*376T= ENSP00000509412.1:n.*376T=
ENST00000692852.1:c.571T= ENSP00000510337.1:p.Cys191=
ENST00000692915.1:c.*778T= ENSP00000508547.1:n.*778T=
ENST00000370396.7:c.571T= MANE Select ENSP00000359423.3:p.Cys191=
ENST00000306167.11:n.438T=
ENST00000370396.6:c.571T= ENSP00000359423.2:p.Cys191=
ENST00000490530.1:n.510T=
NM_000252.2:c.571T= , LRG_839t1:c.571T= NP_000243.1:p.Cys191=
XM_005274687.2:c.571T= XP_005274744.1:p.Cys191=
XM_011531170.1:c.637T= XP_011529472.1:p.Cys213=
XM_011531171.1:c.616T= XP_011529473.1:p.Cys206=
XM_011531172.1:c.616T= XP_011529474.1:p.Cys206=
XM_011531173.1:c.571T= XP_011529475.1:p.Cys191=
XM_011531173.2:c.571T= XP_011529475.1:p.Cys191=
XM_017029547.1:c.616T= XP_016885036.1:p.Cys206=
XM_017029548.1:c.616T= XP_016885037.1:p.Cys206=
XM_017029549.1:c.571T= XP_016885038.1:p.Cys191=
XM_017029550.1:c.460T= XP_016885039.1:p.Cys154=
XM_017029551.2:c.-174T= XP_016885040.1:n.-174T=
NM_000252.3:c.571T= MANE Select NP_000243.1:p.Cys191=
NM_001376906.1:c.571T= NP_001363835.1:p.Cys191=
NM_001376907.1:c.460T= NP_001363836.1:p.Cys154=
NM_001376908.1:c.571T= NP_001363837.1:p.Cys191=