Canonical Allele Identifier: CA271752

Gene: MTM1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150657999G>A , CM000685.2:g.150657999G>A	GRCh38
NC_000023.10:g.149826472G>A , CM000685.1:g.149826472G>A	GRCh37
NC_000023.9:g.149577130G>A	NCBI36
NG_008199.1:g.94426G>A , LRG_839:g.94426G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*765G>A	ENSP00000509844.1:n.*765G>A
ENST00000685439.1:c.887G>A	ENSP00000508454.1:p.Trp296Ter
ENST00000685944.1:c.1232G>A	ENSP00000509266.1:p.Trp411Ter
ENST00000686212.1:n.834G>A
ENST00000687215.1:c.*987G>A	ENSP00000509706.1:n.*987G>A
ENST00000688152.1:c.*676G>A	ENSP00000509360.1:n.*676G>A
ENST00000688403.1:c.488G>A	ENSP00000508944.1:p.Trp163Ter
ENST00000689314.1:c.1277G>A	ENSP00000510607.1:p.Trp426Ter
ENST00000689694.1:c.1232G>A	ENSP00000508718.1:p.Trp411Ter
ENST00000689810.1:c.*881G>A	ENSP00000510635.1:n.*881G>A
ENST00000690282.1:c.488G>A	ENSP00000509809.1:p.Trp163Ter
ENST00000690351.1:c.*884G>A	ENSP00000509728.1:n.*884G>A
ENST00000691232.1:c.887G>A	ENSP00000509675.1:p.Trp296Ter
ENST00000691482.1:n.2247G>A
ENST00000691686.1:c.1232G>A	ENSP00000509784.1:p.Trp411Ter
ENST00000691851.1:c.1053+8098G>A	ENSP00000510106.1:n.1053+8098G>A
ENST00000692015.1:c.1019G>A	ENSP00000510634.1:p.Trp340Ter
ENST00000692638.1:c.*1037G>A	ENSP00000509412.1:n.*1037G>A
ENST00000692852.1:c.1043G>A	ENSP00000510337.1:p.Trp348Ter
ENST00000692915.1:c.*1378G>A	ENSP00000508547.1:n.*1378G>A
ENST00000370396.7:c.1232G>A MANE Select	ENSP00000359423.3:p.Trp411Ter
ENST00000306167.11:n.1099G>A
ENST00000370396.6:c.1232G>A	ENSP00000359423.2:p.Trp411Ter
NM_000252.2:c.1232G>A , LRG_839t1:c.1232G>A	NP_000243.1:p.Trp411Ter
XM_005274687.2:c.1232G>A	XP_005274744.1:p.Trp411Ter
XM_011531170.1:c.1298G>A	XP_011529472.1:p.Trp433Ter
XM_011531171.1:c.1277G>A	XP_011529473.1:p.Trp426Ter
XM_011531172.1:c.1277G>A	XP_011529474.1:p.Trp426Ter
XM_011531173.1:c.1232G>A	XP_011529475.1:p.Trp411Ter
XM_011531173.2:c.1232G>A	XP_011529475.1:p.Trp411Ter
XM_017029547.1:c.1277G>A	XP_016885036.1:p.Trp426Ter
XM_017029548.1:c.1277G>A	XP_016885037.1:p.Trp426Ter
XM_017029549.1:c.1232G>A	XP_016885038.1:p.Trp411Ter
XM_017029550.1:c.1121G>A	XP_016885039.1:p.Trp374Ter
XM_017029551.2:c.488G>A	XP_016885040.1:p.Trp163Ter
NM_000252.3:c.1232G>A MANE Select	NP_000243.1:p.Trp411Ter
NM_001376906.1:c.1232G>A	NP_001363835.1:p.Trp411Ter
NM_001376907.1:c.1121G>A	NP_001363836.1:p.Trp374Ter
NM_001376908.1:c.1232G>A	NP_001363837.1:p.Trp411Ter