Canonical Allele Identifier: CA415256301

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149814165T>G (hg19) ; chrX:g.150645692T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150645692T>G , CM000685.2:g.150645692T>G	GRCh38
NC_000023.10:g.149814165T>G , CM000685.1:g.149814165T>G	GRCh37
NC_000023.9:g.149564823T>G	NCBI36
NG_008199.1:g.82119T>G , LRG_839:g.82119T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*221T>G	ENSP00000509844.1:n.*221T>G
ENST00000685439.1:c.343T>G	ENSP00000508454.1:p.Trp115Gly
ENST00000685944.1:c.688T>G	ENSP00000509266.1:p.Trp230Gly
ENST00000686212.1:n.290T>G
ENST00000687215.1:c.*443T>G	ENSP00000509706.1:n.*443T>G
ENST00000688152.1:c.*132T>G	ENSP00000509360.1:n.*132T>G
ENST00000688403.1:c.-57T>G	ENSP00000508944.1:n.-57T>G
ENST00000689314.1:c.733T>G	ENSP00000510607.1:p.Trp245Gly
ENST00000689694.1:c.688T>G	ENSP00000508718.1:p.Trp230Gly
ENST00000689810.1:c.*337T>G	ENSP00000510635.1:n.*337T>G
ENST00000690282.1:c.-57T>G	ENSP00000509809.1:n.-57T>G
ENST00000690351.1:c.*340T>G	ENSP00000509728.1:n.*340T>G
ENST00000691232.1:c.343T>G	ENSP00000509675.1:p.Trp115Gly
ENST00000691482.1:n.1703T>G
ENST00000691686.1:c.688T>G	ENSP00000509784.1:p.Trp230Gly
ENST00000691851.1:c.688T>G	ENSP00000510106.1:p.Trp230Gly
ENST00000692015.1:c.475T>G	ENSP00000510634.1:p.Trp159Gly
ENST00000692638.1:c.*493T>G	ENSP00000509412.1:n.*493T>G
ENST00000692852.1:c.679-4024T>G	ENSP00000510337.1:n.679-4024T>G
ENST00000692915.1:c.*895T>G	ENSP00000508547.1:n.*895T>G
ENST00000370396.7:c.688T>G MANE Select	ENSP00000359423.3:p.Trp230Gly
ENST00000306167.11:n.555T>G
ENST00000370396.6:c.688T>G	ENSP00000359423.2:p.Trp230Gly
ENST00000490530.1:n.627T>G
NM_000252.2:c.688T>G , LRG_839t1:c.688T>G	NP_000243.1:p.Trp230Gly
XM_005274687.2:c.688T>G	XP_005274744.1:p.Trp230Gly
XM_011531170.1:c.754T>G	XP_011529472.1:p.Trp252Gly
XM_011531171.1:c.733T>G	XP_011529473.1:p.Trp245Gly
XM_011531172.1:c.733T>G	XP_011529474.1:p.Trp245Gly
XM_011531173.1:c.688T>G	XP_011529475.1:p.Trp230Gly
XM_011531173.2:c.688T>G	XP_011529475.1:p.Trp230Gly
XM_017029547.1:c.733T>G	XP_016885036.1:p.Trp245Gly
XM_017029548.1:c.733T>G	XP_016885037.1:p.Trp245Gly
XM_017029549.1:c.688T>G	XP_016885038.1:p.Trp230Gly
XM_017029550.1:c.577T>G	XP_016885039.1:p.Trp193Gly
XM_017029551.2:c.-57T>G	XP_016885040.1:n.-57T>G
NM_000252.3:c.688T>G MANE Select	NP_000243.1:p.Trp230Gly
NM_001376906.1:c.688T>G	NP_001363835.1:p.Trp230Gly
NM_001376907.1:c.577T>G	NP_001363836.1:p.Trp193Gly
NM_001376908.1:c.688T>G	NP_001363837.1:p.Trp230Gly