Canonical Allele Identifier: CA415256042

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149809785G>A (hg19) ; chrX:g.150641312G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150641312G>A , CM000685.2:g.150641312G>A	GRCh38
NC_000023.10:g.149809785G>A , CM000685.1:g.149809785G>A	GRCh37
NC_000023.9:g.149560443G>A	NCBI36
NG_008199.1:g.77739G>A , LRG_839:g.77739G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*105G>A	ENSP00000509844.1:n.*105G>A
ENST00000685439.1:c.227G>A	ENSP00000508454.1:p.Cys76Tyr
ENST00000685944.1:c.572G>A	ENSP00000509266.1:p.Cys191Tyr
ENST00000686212.1:n.174G>A
ENST00000687215.1:c.*327G>A	ENSP00000509706.1:n.*327G>A
ENST00000688152.1:c.*16G>A	ENSP00000509360.1:n.*16G>A
ENST00000688403.1:c.-173G>A	ENSP00000508944.1:n.-173G>A
ENST00000689314.1:c.617G>A	ENSP00000510607.1:p.Cys206Tyr
ENST00000689694.1:c.572G>A	ENSP00000508718.1:p.Cys191Tyr
ENST00000689810.1:c.*221G>A	ENSP00000510635.1:n.*221G>A
ENST00000690282.1:c.-173G>A	ENSP00000509809.1:n.-173G>A
ENST00000690351.1:c.*224G>A	ENSP00000509728.1:n.*224G>A
ENST00000691232.1:c.227G>A	ENSP00000509675.1:p.Cys76Tyr
ENST00000691482.1:n.1587G>A
ENST00000691686.1:c.572G>A	ENSP00000509784.1:p.Cys191Tyr
ENST00000691851.1:c.572G>A	ENSP00000510106.1:p.Cys191Tyr
ENST00000692015.1:c.359G>A	ENSP00000510634.1:p.Cys120Tyr
ENST00000692638.1:c.*377G>A	ENSP00000509412.1:n.*377G>A
ENST00000692852.1:c.572G>A	ENSP00000510337.1:p.Cys191Tyr
ENST00000692915.1:c.*779G>A	ENSP00000508547.1:n.*779G>A
ENST00000370396.7:c.572G>A MANE Select	ENSP00000359423.3:p.Cys191Tyr
ENST00000306167.11:n.439G>A
ENST00000370396.6:c.572G>A	ENSP00000359423.2:p.Cys191Tyr
ENST00000490530.1:n.511G>A
NM_000252.2:c.572G>A , LRG_839t1:c.572G>A	NP_000243.1:p.Cys191Tyr
XM_005274687.2:c.572G>A	XP_005274744.1:p.Cys191Tyr
XM_011531170.1:c.638G>A	XP_011529472.1:p.Cys213Tyr
XM_011531171.1:c.617G>A	XP_011529473.1:p.Cys206Tyr
XM_011531172.1:c.617G>A	XP_011529474.1:p.Cys206Tyr
XM_011531173.1:c.572G>A	XP_011529475.1:p.Cys191Tyr
XM_011531173.2:c.572G>A	XP_011529475.1:p.Cys191Tyr
XM_017029547.1:c.617G>A	XP_016885036.1:p.Cys206Tyr
XM_017029548.1:c.617G>A	XP_016885037.1:p.Cys206Tyr
XM_017029549.1:c.572G>A	XP_016885038.1:p.Cys191Tyr
XM_017029550.1:c.461G>A	XP_016885039.1:p.Cys154Tyr
XM_017029551.2:c.-173G>A	XP_016885040.1:n.-173G>A
NM_000252.3:c.572G>A MANE Select	NP_000243.1:p.Cys191Tyr
NM_001376906.1:c.572G>A	NP_001363835.1:p.Cys191Tyr
NM_001376907.1:c.461G>A	NP_001363836.1:p.Cys154Tyr
NM_001376908.1:c.572G>A	NP_001363837.1:p.Cys191Tyr