Canonical Allele Identifier: CA519111210

Gene: MTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150619127G>T , CM000685.2:g.150619127G>T	GRCh38
NC_000023.10:g.149787600G>T , CM000685.1:g.149787600G>T	GRCh37
NC_000023.9:g.149538258G>T	NCBI36
NG_008199.1:g.55554G>T , LRG_839:g.55554G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.137-19816G>T	ENSP00000509844.1:n.137-19816G>T
ENST00000685439.1:c.87G>T	ENSP00000508454.1:p.Leu29=
ENST00000685944.1:c.432G>T	ENSP00000509266.1:p.Leu144=
ENST00000687215.1:c.147G>T	ENSP00000509706.1:p.Leu49=
ENST00000687365.1:n.487G>T
ENST00000688152.1:c.432G>T	ENSP00000509360.1:p.Leu144=
ENST00000688403.1:c.-300-19816G>T	ENSP00000508944.1:n.-300-19816G>T
ENST00000689314.1:c.477G>T	ENSP00000510607.1:p.Leu159=
ENST00000689694.1:c.432G>T	ENSP00000508718.1:p.Leu144=
ENST00000689810.1:c.432G>T	ENSP00000510635.1:p.Leu144=
ENST00000690282.1:c.-300-19816G>T	ENSP00000509809.1:n.-300-19816G>T
ENST00000690351.1:c.*28G>T	ENSP00000509728.1:n.*28G>T
ENST00000691232.1:c.87G>T	ENSP00000509675.1:p.Leu29=
ENST00000691686.1:c.432G>T	ENSP00000509784.1:p.Leu144=
ENST00000691851.1:c.432G>T	ENSP00000510106.1:p.Leu144=
ENST00000692015.1:c.232-19816G>T	ENSP00000510634.1:n.232-19816G>T
ENST00000692638.1:c.*181G>T	ENSP00000509412.1:n.*181G>T
ENST00000692852.1:c.432G>T	ENSP00000510337.1:p.Leu144=
ENST00000692915.1:c.*427G>T	ENSP00000508547.1:n.*427G>T
ENST00000370396.7:c.432G>T MANE Select	ENSP00000359423.3:p.Leu144=
ENST00000306167.11:n.299G>T
ENST00000370396.6:c.432G>T	ENSP00000359423.2:p.Leu144=
ENST00000424519.1:c.232-19816G>T	ENSP00000400699.1:n.232-19816G>T
ENST00000490530.1:n.371G>T
NM_000252.2:c.432G>T , LRG_839t1:c.432G>T	NP_000243.1:p.Leu144=
XM_005274687.2:c.432G>T	XP_005274744.1:p.Leu144=
XM_011531170.1:c.498G>T	XP_011529472.1:p.Leu166=
XM_011531171.1:c.477G>T	XP_011529473.1:p.Leu159=
XM_011531172.1:c.477G>T	XP_011529474.1:p.Leu159=
XM_011531173.1:c.432G>T	XP_011529475.1:p.Leu144=
XM_011531173.2:c.432G>T	XP_011529475.1:p.Leu144=
XM_017029547.1:c.477G>T	XP_016885036.1:p.Leu159=
XM_017029548.1:c.477G>T	XP_016885037.1:p.Leu159=
XM_017029549.1:c.432G>T	XP_016885038.1:p.Leu144=
XM_017029550.1:c.321G>T	XP_016885039.1:p.Leu107=
NM_000252.3:c.432G>T MANE Select	NP_000243.1:p.Leu144=
NM_001376906.1:c.432G>T	NP_001363835.1:p.Leu144=
NM_001376907.1:c.321G>T	NP_001363836.1:p.Leu107=
NM_001376908.1:c.432G>T	NP_001363837.1:p.Leu144=