Canonical Allele Identifier: CA271950
Gene: MTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159010
ClinVar RCV Id: RCV000146490
dbSNP Id: rs587783863

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150649806T>C , CM000685.2:g.150649806T>C GRCh38
NC_000023.10:g.149818279T>C , CM000685.1:g.149818279T>C GRCh37
NC_000023.9:g.149568937T>C NCBI36
NG_008199.1:g.86233T>C , LRG_839:g.86233T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684910.1:c.*491T>C ENSP00000509844.1:n.*491T>C
ENST00000685439.1:c.613T>C ENSP00000508454.1:p.Ser205Pro
ENST00000685944.1:c.958T>C ENSP00000509266.1:p.Ser320Pro
ENST00000686212.1:n.560T>C
ENST00000687215.1:c.*713T>C ENSP00000509706.1:n.*713T>C
ENST00000688152.1:c.*402T>C ENSP00000509360.1:n.*402T>C
ENST00000688403.1:c.214T>C ENSP00000508944.1:p.Ser72Pro
ENST00000689314.1:c.1003T>C ENSP00000510607.1:p.Ser335Pro
ENST00000689694.1:c.958T>C ENSP00000508718.1:p.Ser320Pro
ENST00000689810.1:c.*607T>C ENSP00000510635.1:n.*607T>C
ENST00000690282.1:c.214T>C ENSP00000509809.1:p.Ser72Pro
ENST00000690351.1:c.*610T>C ENSP00000509728.1:n.*610T>C
ENST00000691232.1:c.613T>C ENSP00000509675.1:p.Ser205Pro
ENST00000691482.1:n.1973T>C
ENST00000691686.1:c.958T>C ENSP00000509784.1:p.Ser320Pro
ENST00000691851.1:c.958T>C ENSP00000510106.1:p.Ser320Pro
ENST00000692015.1:c.745T>C ENSP00000510634.1:p.Ser249Pro
ENST00000692638.1:c.*763T>C ENSP00000509412.1:n.*763T>C
ENST00000692852.1:c.769T>C ENSP00000510337.1:p.Ser257Pro
ENST00000692915.1:c.*1104T>C ENSP00000508547.1:n.*1104T>C
ENST00000370396.7:c.958T>C MANE Select ENSP00000359423.3:p.Ser320Pro
ENST00000306167.11:n.825T>C
ENST00000370396.6:c.958T>C ENSP00000359423.2:p.Ser320Pro
NM_000252.2:c.958T>C , LRG_839t1:c.958T>C NP_000243.1:p.Ser320Pro
XM_005274687.2:c.958T>C XP_005274744.1:p.Ser320Pro
XM_011531170.1:c.1024T>C XP_011529472.1:p.Ser342Pro
XM_011531171.1:c.1003T>C XP_011529473.1:p.Ser335Pro
XM_011531172.1:c.1003T>C XP_011529474.1:p.Ser335Pro
XM_011531173.1:c.958T>C XP_011529475.1:p.Ser320Pro
XM_011531173.2:c.958T>C XP_011529475.1:p.Ser320Pro
XM_017029547.1:c.1003T>C XP_016885036.1:p.Ser335Pro
XM_017029548.1:c.1003T>C XP_016885037.1:p.Ser335Pro
XM_017029549.1:c.958T>C XP_016885038.1:p.Ser320Pro
XM_017029550.1:c.847T>C XP_016885039.1:p.Ser283Pro
XM_017029551.2:c.214T>C XP_016885040.1:p.Ser72Pro
NM_000252.3:c.958T>C MANE Select NP_000243.1:p.Ser320Pro
NM_001376906.1:c.958T>C NP_001363835.1:p.Ser320Pro
NM_001376907.1:c.847T>C NP_001363836.1:p.Ser283Pro
NM_001376908.1:c.958T>C NP_001363837.1:p.Ser320Pro