Canonical Allele Identifier: CA415256105
Gene: MTM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150641338G>C , CM000685.2:g.150641338G>C GRCh38
NC_000023.10:g.149809811G>C , CM000685.1:g.149809811G>C GRCh37
NC_000023.9:g.149560469G>C NCBI36
NG_008199.1:g.77765G>C , LRG_839:g.77765G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684910.1:c.*131G>C ENSP00000509844.1:n.*131G>C
ENST00000685439.1:c.253G>C ENSP00000508454.1:p.Ala85Pro
ENST00000685944.1:c.598G>C ENSP00000509266.1:p.Ala200Pro
ENST00000686212.1:n.200G>C
ENST00000687215.1:c.*353G>C ENSP00000509706.1:n.*353G>C
ENST00000688152.1:c.*42G>C ENSP00000509360.1:n.*42G>C
ENST00000688403.1:c.-147G>C ENSP00000508944.1:n.-147G>C
ENST00000689314.1:c.643G>C ENSP00000510607.1:p.Ala215Pro
ENST00000689694.1:c.598G>C ENSP00000508718.1:p.Ala200Pro
ENST00000689810.1:c.*247G>C ENSP00000510635.1:n.*247G>C
ENST00000690282.1:c.-147G>C ENSP00000509809.1:n.-147G>C
ENST00000690351.1:c.*250G>C ENSP00000509728.1:n.*250G>C
ENST00000691232.1:c.253G>C ENSP00000509675.1:p.Ala85Pro
ENST00000691482.1:n.1613G>C
ENST00000691686.1:c.598G>C ENSP00000509784.1:p.Ala200Pro
ENST00000691851.1:c.598G>C ENSP00000510106.1:p.Ala200Pro
ENST00000692015.1:c.385G>C ENSP00000510634.1:p.Ala129Pro
ENST00000692638.1:c.*403G>C ENSP00000509412.1:n.*403G>C
ENST00000692852.1:c.598G>C ENSP00000510337.1:p.Ala200Pro
ENST00000692915.1:c.*805G>C ENSP00000508547.1:n.*805G>C
ENST00000370396.7:c.598G>C MANE Select ENSP00000359423.3:p.Ala200Pro
ENST00000306167.11:n.465G>C
ENST00000370396.6:c.598G>C ENSP00000359423.2:p.Ala200Pro
ENST00000490530.1:n.537G>C
NM_000252.2:c.598G>C , LRG_839t1:c.598G>C NP_000243.1:p.Ala200Pro
XM_005274687.2:c.598G>C XP_005274744.1:p.Ala200Pro
XM_011531170.1:c.664G>C XP_011529472.1:p.Ala222Pro
XM_011531171.1:c.643G>C XP_011529473.1:p.Ala215Pro
XM_011531172.1:c.643G>C XP_011529474.1:p.Ala215Pro
XM_011531173.1:c.598G>C XP_011529475.1:p.Ala200Pro
XM_011531173.2:c.598G>C XP_011529475.1:p.Ala200Pro
XM_017029547.1:c.643G>C XP_016885036.1:p.Ala215Pro
XM_017029548.1:c.643G>C XP_016885037.1:p.Ala215Pro
XM_017029549.1:c.598G>C XP_016885038.1:p.Ala200Pro
XM_017029550.1:c.487G>C XP_016885039.1:p.Ala163Pro
XM_017029551.2:c.-147G>C XP_016885040.1:n.-147G>C
NM_000252.3:c.598G>C MANE Select NP_000243.1:p.Ala200Pro
NM_001376906.1:c.598G>C NP_001363835.1:p.Ala200Pro
NM_001376907.1:c.487G>C NP_001363836.1:p.Ala163Pro
NM_001376908.1:c.598G>C NP_001363837.1:p.Ala200Pro