Canonical Allele Identifier: CA2465380829
Gene: MTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150641310G= , CM000685.2:g.150641310G= GRCh38
NC_000023.10:g.149809783G= , CM000685.1:g.149809783G= GRCh37
NC_000023.9:g.149560441G= NCBI36
NG_008199.1:g.77737G= , LRG_839:g.77737G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684910.1:c.*103G= ENSP00000509844.1:n.*103G=
ENST00000685439.1:c.225G= ENSP00000508454.1:p.Lys75=
ENST00000685944.1:c.570G= ENSP00000509266.1:p.Lys190=
ENST00000686212.1:n.172G=
ENST00000687215.1:c.*325G= ENSP00000509706.1:n.*325G=
ENST00000688152.1:c.*14G= ENSP00000509360.1:n.*14G=
ENST00000688403.1:c.-175G= ENSP00000508944.1:n.-175G=
ENST00000689314.1:c.615G= ENSP00000510607.1:p.Lys205=
ENST00000689694.1:c.570G= ENSP00000508718.1:p.Lys190=
ENST00000689810.1:c.*219G= ENSP00000510635.1:n.*219G=
ENST00000690282.1:c.-175G= ENSP00000509809.1:n.-175G=
ENST00000690351.1:c.*222G= ENSP00000509728.1:n.*222G=
ENST00000691232.1:c.225G= ENSP00000509675.1:p.Lys75=
ENST00000691482.1:n.1585G=
ENST00000691686.1:c.570G= ENSP00000509784.1:p.Lys190=
ENST00000691851.1:c.570G= ENSP00000510106.1:p.Lys190=
ENST00000692015.1:c.357G= ENSP00000510634.1:p.Lys119=
ENST00000692638.1:c.*375G= ENSP00000509412.1:n.*375G=
ENST00000692852.1:c.570G= ENSP00000510337.1:p.Lys190=
ENST00000692915.1:c.*777G= ENSP00000508547.1:n.*777G=
ENST00000370396.7:c.570G= MANE Select ENSP00000359423.3:p.Lys190=
ENST00000306167.11:n.437G=
ENST00000370396.6:c.570G= ENSP00000359423.2:p.Lys190=
ENST00000490530.1:n.509G=
NM_000252.2:c.570G= , LRG_839t1:c.570G= NP_000243.1:p.Lys190=
XM_005274687.2:c.570G= XP_005274744.1:p.Lys190=
XM_011531170.1:c.636G= XP_011529472.1:p.Lys212=
XM_011531171.1:c.615G= XP_011529473.1:p.Lys205=
XM_011531172.1:c.615G= XP_011529474.1:p.Lys205=
XM_011531173.1:c.570G= XP_011529475.1:p.Lys190=
XM_011531173.2:c.570G= XP_011529475.1:p.Lys190=
XM_017029547.1:c.615G= XP_016885036.1:p.Lys205=
XM_017029548.1:c.615G= XP_016885037.1:p.Lys205=
XM_017029549.1:c.570G= XP_016885038.1:p.Lys190=
XM_017029550.1:c.459G= XP_016885039.1:p.Lys153=
XM_017029551.2:c.-175G= XP_016885040.1:n.-175G=
NM_000252.3:c.570G= MANE Select NP_000243.1:p.Lys190=
NM_001376906.1:c.570G= NP_001363835.1:p.Lys190=
NM_001376907.1:c.459G= NP_001363836.1:p.Lys153=
NM_001376908.1:c.570G= NP_001363837.1:p.Lys190=