Canonical Allele Identifier: CA2579721094

Gene: MTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150641350del , CM000685.2:g.150641350del	GRCh38
NC_000023.10:g.149809823del , CM000685.1:g.149809823del	GRCh37
NC_000023.9:g.149560481del	NCBI36
NG_008199.1:g.77777del , LRG_839:g.77777del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*143del	ENSP00000509844.1:n.*143del
ENST00000685439.1:c.265del	ENSP00000508454.1:p.Val89PhefsTer?
ENST00000685944.1:c.610del	ENSP00000509266.1:p.Val204PhefsTer?
ENST00000686212.1:n.212del
ENST00000687215.1:c.*365del	ENSP00000509706.1:n.*365del
ENST00000688152.1:c.*54del	ENSP00000509360.1:n.*54del
ENST00000688403.1:c.-135del	ENSP00000508944.1:n.-135del
ENST00000689314.1:c.655del	ENSP00000510607.1:p.Val219PhefsTer?
ENST00000689694.1:c.610del	ENSP00000508718.1:p.Val204PhefsTer?
ENST00000689810.1:c.*259del	ENSP00000510635.1:n.*259del
ENST00000690282.1:c.-135del	ENSP00000509809.1:n.-135del
ENST00000690351.1:c.*262del	ENSP00000509728.1:n.*262del
ENST00000691232.1:c.265del	ENSP00000509675.1:p.Val89PhefsTer?
ENST00000691482.1:n.1625del
ENST00000691686.1:c.610del	ENSP00000509784.1:p.Val204PhefsTer?
ENST00000691851.1:c.610del	ENSP00000510106.1:p.Val204PhefsTer?
ENST00000692015.1:c.397del	ENSP00000510634.1:p.Val133PhefsTer?
ENST00000692638.1:c.*415del	ENSP00000509412.1:n.*415del
ENST00000692852.1:c.610del	ENSP00000510337.1:p.Val204PhefsTer?
ENST00000692915.1:c.*817del	ENSP00000508547.1:n.*817del
ENST00000370396.7:c.610del MANE Select	ENSP00000359423.3:p.Val204PhefsTer?
ENST00000306167.11:n.477del
ENST00000370396.6:c.610del	ENSP00000359423.2:p.Val204PhefsTer?
ENST00000490530.1:n.549del
NM_000252.2:c.610del , LRG_839t1:c.610del	NP_000243.1:p.Val204PhefsTer?
XM_005274687.2:c.610del	XP_005274744.1:p.Val204PhefsTer?
XM_011531170.1:c.676del	XP_011529472.1:p.Val226PhefsTer?
XM_011531171.1:c.655del	XP_011529473.1:p.Val219PhefsTer?
XM_011531172.1:c.655del	XP_011529474.1:p.Val219PhefsTer?
XM_011531173.1:c.610del	XP_011529475.1:p.Val204PhefsTer?
XM_011531173.2:c.610del	XP_011529475.1:p.Val204PhefsTer?
XM_017029547.1:c.655del	XP_016885036.1:p.Val219PhefsTer?
XM_017029548.1:c.655del	XP_016885037.1:p.Val219PhefsTer?
XM_017029549.1:c.610del	XP_016885038.1:p.Val204PhefsTer?
XM_017029550.1:c.499del	XP_016885039.1:p.Val167PhefsTer?
XM_017029551.2:c.-135del	XP_016885040.1:n.-135del
NM_000252.3:c.610del MANE Select	NP_000243.1:p.Val204PhefsTer?
NM_001376906.1:c.610del	NP_001363835.1:p.Val204PhefsTer?
NM_001376907.1:c.499del	NP_001363836.1:p.Val167PhefsTer?
NM_001376908.1:c.610del	NP_001363837.1:p.Val204PhefsTer?