Canonical Allele Identifier: CA415259667

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149828884T>G (hg19) ; chrX:g.150660411T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150660411T>G , CM000685.2:g.150660411T>G	GRCh38
NC_000023.10:g.149828884T>G , CM000685.1:g.149828884T>G	GRCh37
NC_000023.9:g.149579542T>G	NCBI36
NG_008199.1:g.96838T>G , LRG_839:g.96838T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*927T>G	ENSP00000509844.1:n.*927T>G
ENST00000685439.1:c.1049T>G	ENSP00000508454.1:p.Ile350Arg
ENST00000685944.1:c.1394T>G	ENSP00000509266.1:p.Ile465Arg
ENST00000686212.1:n.996T>G
ENST00000687215.1:c.*1149T>G	ENSP00000509706.1:n.*1149T>G
ENST00000688152.1:c.*838T>G	ENSP00000509360.1:n.*838T>G
ENST00000688403.1:c.650T>G	ENSP00000508944.1:p.Ile217Arg
ENST00000689314.1:c.1439T>G	ENSP00000510607.1:p.Ile480Arg
ENST00000689694.1:c.1394T>G	ENSP00000508718.1:p.Ile465Arg
ENST00000689810.1:c.*1043T>G	ENSP00000510635.1:n.*1043T>G
ENST00000690282.1:c.650T>G	ENSP00000509809.1:p.Ile217Arg
ENST00000690351.1:c.*1046T>G	ENSP00000509728.1:n.*1046T>G
ENST00000691232.1:c.1049T>G	ENSP00000509675.1:p.Ile350Arg
ENST00000691482.1:n.2409T>G
ENST00000691686.1:c.1301T>G	ENSP00000509784.1:p.Ile434Arg
ENST00000691851.1:c.1053+10510T>G	ENSP00000510106.1:n.1053+10510T>G
ENST00000692015.1:c.1181T>G	ENSP00000510634.1:p.Ile394Arg
ENST00000692638.1:c.*1192T>G	ENSP00000509412.1:n.*1192T>G
ENST00000692852.1:c.1205T>G	ENSP00000510337.1:p.Ile402Arg
ENST00000692915.1:c.*1540T>G	ENSP00000508547.1:n.*1540T>G
ENST00000370396.7:c.1394T>G MANE Select	ENSP00000359423.3:p.Ile465Arg
ENST00000306167.11:n.1261T>G
ENST00000370396.6:c.1394T>G	ENSP00000359423.2:p.Ile465Arg
NM_000252.2:c.1394T>G , LRG_839t1:c.1394T>G	NP_000243.1:p.Ile465Arg
XM_005274687.2:c.1394T>G	XP_005274744.1:p.Ile465Arg
XM_011531170.1:c.1460T>G	XP_011529472.1:p.Ile487Arg
XM_011531171.1:c.1439T>G	XP_011529473.1:p.Ile480Arg
XM_011531172.1:c.1439T>G	XP_011529474.1:p.Ile480Arg
XM_011531173.1:c.1394T>G	XP_011529475.1:p.Ile465Arg
XM_011531173.2:c.1394T>G	XP_011529475.1:p.Ile465Arg
XM_017029547.1:c.1439T>G	XP_016885036.1:p.Ile480Arg
XM_017029548.1:c.1439T>G	XP_016885037.1:p.Ile480Arg
XM_017029549.1:c.1394T>G	XP_016885038.1:p.Ile465Arg
XM_017029550.1:c.1283T>G	XP_016885039.1:p.Ile428Arg
XM_017029551.2:c.650T>G	XP_016885040.1:p.Ile217Arg
NM_000252.3:c.1394T>G MANE Select	NP_000243.1:p.Ile465Arg
NM_001376906.1:c.1394T>G	NP_001363835.1:p.Ile465Arg
NM_001376907.1:c.1283T>G	NP_001363836.1:p.Ile428Arg
NM_001376908.1:c.1394T>G	NP_001363837.1:p.Ile465Arg