Canonical Allele Identifier: CA415256255
Gene: MTM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150641413A>T , CM000685.2:g.150641413A>T GRCh38
NC_000023.10:g.149809886A>T , CM000685.1:g.149809886A>T GRCh37
NC_000023.9:g.149560544A>T NCBI36
NG_008199.1:g.77840A>T , LRG_839:g.77840A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684910.1:c.*206A>T ENSP00000509844.1:n.*206A>T
ENST00000685439.1:c.328A>T ENSP00000508454.1:p.Ile110Phe
ENST00000685944.1:c.673A>T ENSP00000509266.1:p.Ile225Phe
ENST00000686212.1:n.275A>T
ENST00000687215.1:c.*428A>T ENSP00000509706.1:n.*428A>T
ENST00000688152.1:c.*117A>T ENSP00000509360.1:n.*117A>T
ENST00000688403.1:c.-72A>T ENSP00000508944.1:n.-72A>T
ENST00000689314.1:c.718A>T ENSP00000510607.1:p.Ile240Phe
ENST00000689694.1:c.673A>T ENSP00000508718.1:p.Ile225Phe
ENST00000689810.1:c.*322A>T ENSP00000510635.1:n.*322A>T
ENST00000690282.1:c.-72A>T ENSP00000509809.1:n.-72A>T
ENST00000690351.1:c.*325A>T ENSP00000509728.1:n.*325A>T
ENST00000691232.1:c.328A>T ENSP00000509675.1:p.Ile110Phe
ENST00000691482.1:n.1688A>T
ENST00000691686.1:c.673A>T ENSP00000509784.1:p.Ile225Phe
ENST00000691851.1:c.673A>T ENSP00000510106.1:p.Ile225Phe
ENST00000692015.1:c.460A>T ENSP00000510634.1:p.Ile154Phe
ENST00000692638.1:c.*478A>T ENSP00000509412.1:n.*478A>T
ENST00000692852.1:c.673A>T ENSP00000510337.1:p.Ile225Phe
ENST00000692915.1:c.*880A>T ENSP00000508547.1:n.*880A>T
ENST00000370396.7:c.673A>T MANE Select ENSP00000359423.3:p.Ile225Phe
ENST00000306167.11:n.540A>T
ENST00000370396.6:c.673A>T ENSP00000359423.2:p.Ile225Phe
ENST00000490530.1:n.612A>T
NM_000252.2:c.673A>T , LRG_839t1:c.673A>T NP_000243.1:p.Ile225Phe
XM_005274687.2:c.673A>T XP_005274744.1:p.Ile225Phe
XM_011531170.1:c.739A>T XP_011529472.1:p.Ile247Phe
XM_011531171.1:c.718A>T XP_011529473.1:p.Ile240Phe
XM_011531172.1:c.718A>T XP_011529474.1:p.Ile240Phe
XM_011531173.1:c.673A>T XP_011529475.1:p.Ile225Phe
XM_011531173.2:c.673A>T XP_011529475.1:p.Ile225Phe
XM_017029547.1:c.718A>T XP_016885036.1:p.Ile240Phe
XM_017029548.1:c.718A>T XP_016885037.1:p.Ile240Phe
XM_017029549.1:c.673A>T XP_016885038.1:p.Ile225Phe
XM_017029550.1:c.562A>T XP_016885039.1:p.Ile188Phe
XM_017029551.2:c.-72A>T XP_016885040.1:n.-72A>T
NM_000252.3:c.673A>T MANE Select NP_000243.1:p.Ile225Phe
NM_001376906.1:c.673A>T NP_001363835.1:p.Ile225Phe
NM_001376907.1:c.562A>T NP_001363836.1:p.Ile188Phe
NM_001376908.1:c.673A>T NP_001363837.1:p.Ile225Phe