Canonical Allele Identifier: CA10539288

Gene: MTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150663434A>G , CM000685.2:g.150663434A>G	GRCh38
NC_000023.10:g.149831907A>G , CM000685.1:g.149831907A>G	GRCh37
NC_000023.9:g.149582565A>G	NCBI36
NG_008199.1:g.99861A>G , LRG_839:g.99861A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*1002A>G	ENSP00000509844.1:n.*1002A>G
ENST00000685439.1:c.1124A>G	ENSP00000508454.1:p.Lys375Arg
ENST00000685944.1:c.1469A>G	ENSP00000509266.1:p.Lys490Arg
ENST00000686212.1:n.1071A>G
ENST00000687215.1:c.*1224A>G	ENSP00000509706.1:n.*1224A>G
ENST00000688152.1:c.*913A>G	ENSP00000509360.1:n.*913A>G
ENST00000688403.1:c.725A>G	ENSP00000508944.1:p.Lys242Arg
ENST00000689314.1:c.1514A>G	ENSP00000510607.1:p.Lys505Arg
ENST00000689694.1:c.1469A>G	ENSP00000508718.1:p.Lys490Arg
ENST00000689810.1:c.*1118A>G	ENSP00000510635.1:n.*1118A>G
ENST00000690282.1:c.725A>G	ENSP00000509809.1:p.Lys242Arg
ENST00000690351.1:c.*1121A>G	ENSP00000509728.1:n.*1121A>G
ENST00000691232.1:c.1124A>G	ENSP00000509675.1:p.Lys375Arg
ENST00000691482.1:n.5432A>G
ENST00000691686.1:c.1376A>G	ENSP00000509784.1:p.Lys459Arg
ENST00000691851.1:c.1054-7994A>G	ENSP00000510106.1:n.1054-7994A>G
ENST00000692015.1:c.1256A>G	ENSP00000510634.1:p.Lys419Arg
ENST00000692638.1:c.*1267A>G	ENSP00000509412.1:n.*1267A>G
ENST00000692852.1:c.1280A>G	ENSP00000510337.1:p.Lys427Arg
ENST00000692915.1:c.*1615A>G	ENSP00000508547.1:n.*1615A>G
ENST00000370396.7:c.1469A>G MANE Select	ENSP00000359423.3:p.Lys490Arg
ENST00000306167.11:n.1336A>G
ENST00000370396.6:c.1469A>G	ENSP00000359423.2:p.Lys490Arg
NM_000252.2:c.1469A>G , LRG_839t1:c.1469A>G	NP_000243.1:p.Lys490Arg
XM_005274687.2:c.1469A>G	XP_005274744.1:p.Lys490Arg
XM_011531170.1:c.1535A>G	XP_011529472.1:p.Lys512Arg
XM_011531171.1:c.1514A>G	XP_011529473.1:p.Lys505Arg
XM_011531172.1:c.1514A>G	XP_011529474.1:p.Lys505Arg
XM_011531173.1:c.1469A>G	XP_011529475.1:p.Lys490Arg
XM_011531173.2:c.1469A>G	XP_011529475.1:p.Lys490Arg
XM_017029547.1:c.1514A>G	XP_016885036.1:p.Lys505Arg
XM_017029548.1:c.1514A>G	XP_016885037.1:p.Lys505Arg
XM_017029549.1:c.1469A>G	XP_016885038.1:p.Lys490Arg
XM_017029550.1:c.1358A>G	XP_016885039.1:p.Lys453Arg
XM_017029551.2:c.725A>G	XP_016885040.1:p.Lys242Arg
NM_000252.3:c.1469A>G MANE Select	NP_000243.1:p.Lys490Arg
NM_001376906.1:c.1469A>G	NP_001363835.1:p.Lys490Arg
NM_001376907.1:c.1358A>G	NP_001363836.1:p.Lys453Arg
NM_001376908.1:c.1469A>G	NP_001363837.1:p.Lys490Arg