Canonical Allele Identifier: CA415256323

Gene: MTM1

Linked Data

• MyVariant Identifiers: chrX:g.149814174C>T (hg19) ; chrX:g.150645701C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150645701C>T , CM000685.2:g.150645701C>T	GRCh38
NC_000023.10:g.149814174C>T , CM000685.1:g.149814174C>T	GRCh37
NC_000023.9:g.149564832C>T	NCBI36
NG_008199.1:g.82128C>T , LRG_839:g.82128C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*230C>T	ENSP00000509844.1:n.*230C>T
ENST00000685439.1:c.352C>T	ENSP00000508454.1:p.Pro118Ser
ENST00000685944.1:c.697C>T	ENSP00000509266.1:p.Pro233Ser
ENST00000686212.1:n.299C>T
ENST00000687215.1:c.*452C>T	ENSP00000509706.1:n.*452C>T
ENST00000688152.1:c.*141C>T	ENSP00000509360.1:n.*141C>T
ENST00000688403.1:c.-48C>T	ENSP00000508944.1:n.-48C>T
ENST00000689314.1:c.742C>T	ENSP00000510607.1:p.Pro248Ser
ENST00000689694.1:c.697C>T	ENSP00000508718.1:p.Pro233Ser
ENST00000689810.1:c.*346C>T	ENSP00000510635.1:n.*346C>T
ENST00000690282.1:c.-48C>T	ENSP00000509809.1:n.-48C>T
ENST00000690351.1:c.*349C>T	ENSP00000509728.1:n.*349C>T
ENST00000691232.1:c.352C>T	ENSP00000509675.1:p.Pro118Ser
ENST00000691482.1:n.1712C>T
ENST00000691686.1:c.697C>T	ENSP00000509784.1:p.Pro233Ser
ENST00000691851.1:c.697C>T	ENSP00000510106.1:p.Pro233Ser
ENST00000692015.1:c.484C>T	ENSP00000510634.1:p.Pro162Ser
ENST00000692638.1:c.*502C>T	ENSP00000509412.1:n.*502C>T
ENST00000692852.1:c.679-4015C>T	ENSP00000510337.1:n.679-4015C>T
ENST00000692915.1:c.*904C>T	ENSP00000508547.1:n.*904C>T
ENST00000370396.7:c.697C>T MANE Select	ENSP00000359423.3:p.Pro233Ser
ENST00000306167.11:n.564C>T
ENST00000370396.6:c.697C>T	ENSP00000359423.2:p.Pro233Ser
ENST00000490530.1:n.636C>T
NM_000252.2:c.697C>T , LRG_839t1:c.697C>T	NP_000243.1:p.Pro233Ser
XM_005274687.2:c.697C>T	XP_005274744.1:p.Pro233Ser
XM_011531170.1:c.763C>T	XP_011529472.1:p.Pro255Ser
XM_011531171.1:c.742C>T	XP_011529473.1:p.Pro248Ser
XM_011531172.1:c.742C>T	XP_011529474.1:p.Pro248Ser
XM_011531173.1:c.697C>T	XP_011529475.1:p.Pro233Ser
XM_011531173.2:c.697C>T	XP_011529475.1:p.Pro233Ser
XM_017029547.1:c.742C>T	XP_016885036.1:p.Pro248Ser
XM_017029548.1:c.742C>T	XP_016885037.1:p.Pro248Ser
XM_017029549.1:c.697C>T	XP_016885038.1:p.Pro233Ser
XM_017029550.1:c.586C>T	XP_016885039.1:p.Pro196Ser
XM_017029551.2:c.-48C>T	XP_016885040.1:n.-48C>T
NM_000252.3:c.697C>T MANE Select	NP_000243.1:p.Pro233Ser
NM_001376906.1:c.697C>T	NP_001363835.1:p.Pro233Ser
NM_001376907.1:c.586C>T	NP_001363836.1:p.Pro196Ser
NM_001376908.1:c.697C>T	NP_001363837.1:p.Pro233Ser