Canonical Allele Identifier: CA920448036

Gene: MTM1

Linked Data

• dbSNP Id: rs1557413843
• gnomAD v4: X-150641192-GGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150641196_150641198del , CM000685.2:g.150641196_150641198del	GRCh38
NC_000023.10:g.149809669_149809671del , CM000685.1:g.149809669_149809671del	GRCh37
NC_000023.9:g.149560327_149560329del	NCBI36
NG_008199.1:g.77623_77625del , LRG_839:g.77623_77625del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684910.1:c.*62-73_*62-71del	ENSP00000509844.1:n.*62-73_*62-71del
ENST00000685439.1:c.184-73_184-71del	ENSP00000508454.1:n.184-73_184-71del
ENST00000685944.1:c.529-73_529-71del	ENSP00000509266.1:n.529-73_529-71del
ENST00000686212.1:n.58_60del
ENST00000687215.1:c.*284-73_*284-71del	ENSP00000509706.1:n.*284-73_*284-71del
ENST00000688152.1:c.585-73_585-71del	ENSP00000509360.1:n.585-73_585-71del
ENST00000688403.1:c.-216-73_-216-71del	ENSP00000508944.1:n.-216-73_-216-71del
ENST00000689314.1:c.574-73_574-71del	ENSP00000510607.1:n.574-73_574-71del
ENST00000689694.1:c.529-73_529-71del	ENSP00000508718.1:n.529-73_529-71del
ENST00000689810.1:c.*178-73_*178-71del	ENSP00000510635.1:n.*178-73_*178-71del
ENST00000690282.1:c.-216-73_-216-71del	ENSP00000509809.1:n.-216-73_-216-71del
ENST00000690351.1:c.*181-73_*181-71del	ENSP00000509728.1:n.*181-73_*181-71del
ENST00000691232.1:c.184-73_184-71del	ENSP00000509675.1:n.184-73_184-71del
ENST00000691482.1:n.1471_1473del
ENST00000691686.1:c.529-73_529-71del	ENSP00000509784.1:n.529-73_529-71del
ENST00000691851.1:c.529-73_529-71del	ENSP00000510106.1:n.529-73_529-71del
ENST00000692015.1:c.316-73_316-71del	ENSP00000510634.1:n.316-73_316-71del
ENST00000692638.1:c.*334-73_*334-71del	ENSP00000509412.1:n.*334-73_*334-71del
ENST00000692852.1:c.529-73_529-71del	ENSP00000510337.1:n.529-73_529-71del
ENST00000692915.1:c.*736-73_*736-71del	ENSP00000508547.1:n.*736-73_*736-71del
ENST00000370396.7:c.529-73_529-71del MANE Select	ENSP00000359423.3:n.529-73_529-71del
ENST00000306167.11:n.396-73_396-71del
ENST00000370396.6:c.529-73_529-71del	ENSP00000359423.2:n.529-73_529-71del
ENST00000490530.1:n.468-73_468-71del
NM_000252.2:c.529-73_529-71del , LRG_839t1:c.529-73_529-71del	NP_000243.1:n.529-73_529-71del
XM_005274687.2:c.529-73_529-71del	XP_005274744.1:n.529-73_529-71del
XM_011531170.1:c.595-73_595-71del	XP_011529472.1:n.595-73_595-71del
XM_011531171.1:c.574-73_574-71del	XP_011529473.1:n.574-73_574-71del
XM_011531172.1:c.574-73_574-71del	XP_011529474.1:n.574-73_574-71del
XM_011531173.1:c.529-73_529-71del	XP_011529475.1:n.529-73_529-71del
XM_011531173.2:c.529-73_529-71del	XP_011529475.1:n.529-73_529-71del
XM_017029547.1:c.574-73_574-71del	XP_016885036.1:n.574-73_574-71del
XM_017029548.1:c.574-73_574-71del	XP_016885037.1:n.574-73_574-71del
XM_017029549.1:c.529-73_529-71del	XP_016885038.1:n.529-73_529-71del
XM_017029550.1:c.418-73_418-71del	XP_016885039.1:n.418-73_418-71del
XM_017029551.2:c.-216-73_-216-71del	XP_016885040.1:n.-216-73_-216-71del
NM_000252.3:c.529-73_529-71del MANE Select	NP_000243.1:n.529-73_529-71del
NM_001376906.1:c.529-73_529-71del	NP_001363835.1:n.529-73_529-71del
NM_001376907.1:c.418-73_418-71del	NP_001363836.1:n.418-73_418-71del
NM_001376908.1:c.529-73_529-71del	NP_001363837.1:n.529-73_529-71del