Canonical Allele Identifier: CA415259810

Gene: MTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150660476G>T , CM000685.2:g.150660476G>T	GRCh38
NC_000023.10:g.149828949G>T , CM000685.1:g.149828949G>T	GRCh37
NC_000023.9:g.149579607G>T	NCBI36
NG_008199.1:g.96903G>T , LRG_839:g.96903G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000252.3:c.1459G>T MANE Select	NP_000243.1:p.Glu487Ter
ENST00000370396.7:c.1459G>T MANE Select	ENSP00000359423.3:p.Glu487Ter
NM_000252.2:c.1459G>T , LRG_839t1:c.1459G>T	NP_000243.1:p.Glu487Ter
NM_001376906.1:c.1459G>T	NP_001363835.1:p.Glu487Ter
NM_001376907.1:c.1348G>T	NP_001363836.1:p.Glu450Ter
NM_001376908.1:c.1459G>T	NP_001363837.1:p.Glu487Ter
ENST00000306167.11:n.1326G>T
ENST00000370396.6:c.1459G>T	ENSP00000359423.2:p.Glu487Ter
ENST00000684910.1:c.*992G>T	ENSP00000509844.1:n.*992G>T
ENST00000685439.1:c.1114G>T	ENSP00000508454.1:p.Glu372Ter
ENST00000685944.1:c.1459G>T	ENSP00000509266.1:p.Glu487Ter
ENST00000686212.1:n.1061G>T
ENST00000687215.1:c.*1214G>T	ENSP00000509706.1:n.*1214G>T
ENST00000688152.1:c.*903G>T	ENSP00000509360.1:n.*903G>T
ENST00000688403.1:c.715G>T	ENSP00000508944.1:p.Glu239Ter
ENST00000689314.1:c.1504G>T	ENSP00000510607.1:p.Glu502Ter
ENST00000689694.1:c.1459G>T	ENSP00000508718.1:p.Glu487Ter
ENST00000689810.1:c.*1108G>T	ENSP00000510635.1:n.*1108G>T
ENST00000690282.1:c.715G>T	ENSP00000509809.1:p.Glu239Ter
ENST00000690351.1:c.*1111G>T	ENSP00000509728.1:n.*1111G>T
ENST00000691232.1:c.1114G>T	ENSP00000509675.1:p.Glu372Ter
ENST00000691482.1:n.2474G>T
ENST00000691686.1:c.1366G>T	ENSP00000509784.1:p.Glu456Ter
ENST00000691851.1:c.1053+10575G>T	ENSP00000510106.1:n.1053+10575G>T
ENST00000692015.1:c.1246G>T	ENSP00000510634.1:p.Glu416Ter
ENST00000692638.1:c.*1257G>T	ENSP00000509412.1:n.*1257G>T
ENST00000692852.1:c.1270G>T	ENSP00000510337.1:p.Glu424Ter
ENST00000692915.1:c.*1605G>T	ENSP00000508547.1:n.*1605G>T
XM_005274687.2:c.1459G>T	XP_005274744.1:p.Glu487Ter
XM_011531170.1:c.1525G>T	XP_011529472.1:p.Glu509Ter
XM_011531171.1:c.1504G>T	XP_011529473.1:p.Glu502Ter
XM_011531172.1:c.1504G>T	XP_011529474.1:p.Glu502Ter
XM_011531173.1:c.1459G>T	XP_011529475.1:p.Glu487Ter
XM_011531173.2:c.1459G>T	XP_011529475.1:p.Glu487Ter
XM_017029547.1:c.1504G>T	XP_016885036.1:p.Glu502Ter
XM_017029548.1:c.1504G>T	XP_016885037.1:p.Glu502Ter
XM_017029549.1:c.1459G>T	XP_016885038.1:p.Glu487Ter
XM_017029550.1:c.1348G>T	XP_016885039.1:p.Glu450Ter
XM_017029551.2:c.715G>T	XP_016885040.1:p.Glu239Ter