Canonical Allele Identifier: CA2465382028

Gene: MTM1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150645624T= , CM000685.2:g.150645624T=	GRCh38
NC_000023.10:g.149814097T= , CM000685.1:g.149814097T=	GRCh37
NC_000023.9:g.149564755T=	NCBI36
NG_008199.1:g.82051T= , LRG_839:g.82051T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*212-59T=	ENSP00000509844.1:n.*212-59T=
ENST00000685439.1:c.334-59T=	ENSP00000508454.1:n.334-59T=
ENST00000685944.1:c.679-59T=	ENSP00000509266.1:n.679-59T=
ENST00000686212.1:n.281-59T=
ENST00000687215.1:c.*434-59T=	ENSP00000509706.1:n.*434-59T=
ENST00000688152.1:c.*123-59T=	ENSP00000509360.1:n.*123-59T=
ENST00000688403.1:c.-66-59T=	ENSP00000508944.1:n.-66-59T=
ENST00000689314.1:c.724-59T=	ENSP00000510607.1:n.724-59T=
ENST00000689694.1:c.679-59T=	ENSP00000508718.1:n.679-59T=
ENST00000689810.1:c.*328-59T=	ENSP00000510635.1:n.*328-59T=
ENST00000690282.1:c.-66-59T=	ENSP00000509809.1:n.-66-59T=
ENST00000690351.1:c.*331-59T=	ENSP00000509728.1:n.*331-59T=
ENST00000691232.1:c.334-59T=	ENSP00000509675.1:n.334-59T=
ENST00000691482.1:n.1694-59T=
ENST00000691686.1:c.679-59T=	ENSP00000509784.1:n.679-59T=
ENST00000691851.1:c.679-59T=	ENSP00000510106.1:n.679-59T=
ENST00000692015.1:c.466-59T=	ENSP00000510634.1:n.466-59T=
ENST00000692638.1:c.*484-59T=	ENSP00000509412.1:n.*484-59T=
ENST00000692852.1:c.679-4092T=	ENSP00000510337.1:n.679-4092T=
ENST00000692915.1:c.*886-59T=	ENSP00000508547.1:n.*886-59T=
ENST00000370396.7:c.679-59T= MANE Select	ENSP00000359423.3:n.679-59T=
ENST00000306167.11:n.546-59T=
ENST00000370396.6:c.679-59T=	ENSP00000359423.2:n.679-59T=
ENST00000490530.1:n.618-59T=
NM_000252.2:c.679-59T= , LRG_839t1:c.679-59T=	NP_000243.1:n.679-59T=
XM_005274687.2:c.679-59T=	XP_005274744.1:n.679-59T=
XM_011531170.1:c.745-59T=	XP_011529472.1:n.745-59T=
XM_011531171.1:c.724-59T=	XP_011529473.1:n.724-59T=
XM_011531172.1:c.724-59T=	XP_011529474.1:n.724-59T=
XM_011531173.1:c.679-59T=	XP_011529475.1:n.679-59T=
XM_011531173.2:c.679-59T=	XP_011529475.1:n.679-59T=
XM_017029547.1:c.724-59T=	XP_016885036.1:n.724-59T=
XM_017029548.1:c.724-59T=	XP_016885037.1:n.724-59T=
XM_017029549.1:c.679-59T=	XP_016885038.1:n.679-59T=
XM_017029550.1:c.568-59T=	XP_016885039.1:n.568-59T=
XM_017029551.2:c.-66-59T=	XP_016885040.1:n.-66-59T=
NM_000252.3:c.679-59T= MANE Select	NP_000243.1:n.679-59T=
NM_001376906.1:c.679-59T=	NP_001363835.1:n.679-59T=
NM_001376907.1:c.568-59T=	NP_001363836.1:n.568-59T=
NM_001376908.1:c.679-59T=	NP_001363837.1:n.679-59T=