Canonical Allele Identifier: CA1138387080

Gene: MTM1

Linked Data

• dbSNP Id: rs2040198169
• gnomAD v3: X-150660337-GT-G
• gnomAD v4: X-150660337-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150660342del , CM000685.2:g.150660342del	GRCh38
NC_000023.10:g.149828815del , CM000685.1:g.149828815del	GRCh37
NC_000023.9:g.149579473del	NCBI36
NG_008199.1:g.96769del , LRG_839:g.96769del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684910.1:c.*887-29del	ENSP00000509844.1:n.*887-29del
ENST00000685439.1:c.1009-29del	ENSP00000508454.1:n.1009-29del
ENST00000685944.1:c.1354-29del	ENSP00000509266.1:n.1354-29del
ENST00000686212.1:n.956-29del
ENST00000687215.1:c.*1109-29del	ENSP00000509706.1:n.*1109-29del
ENST00000688152.1:c.*798-29del	ENSP00000509360.1:n.*798-29del
ENST00000688403.1:c.610-29del	ENSP00000508944.1:n.610-29del
ENST00000689314.1:c.1399-29del	ENSP00000510607.1:n.1399-29del
ENST00000689694.1:c.1354-29del	ENSP00000508718.1:n.1354-29del
ENST00000689810.1:c.*1003-29del	ENSP00000510635.1:n.*1003-29del
ENST00000690282.1:c.610-29del	ENSP00000509809.1:n.610-29del
ENST00000690351.1:c.*1006-29del	ENSP00000509728.1:n.*1006-29del
ENST00000691232.1:c.1009-29del	ENSP00000509675.1:n.1009-29del
ENST00000691482.1:n.2369-29del
ENST00000691686.1:c.1261-29del	ENSP00000509784.1:n.1261-29del
ENST00000691851.1:c.1053+10441del	ENSP00000510106.1:n.1053+10441del
ENST00000692015.1:c.1141-29del	ENSP00000510634.1:n.1141-29del
ENST00000692638.1:c.*1152-29del	ENSP00000509412.1:n.*1152-29del
ENST00000692852.1:c.1165-29del	ENSP00000510337.1:n.1165-29del
ENST00000692915.1:c.*1500-29del	ENSP00000508547.1:n.*1500-29del
ENST00000370396.7:c.1354-29del MANE Select	ENSP00000359423.3:n.1354-29del
ENST00000306167.11:n.1221-29del
ENST00000370396.6:c.1354-29del	ENSP00000359423.2:n.1354-29del
NM_000252.2:c.1354-29del , LRG_839t1:c.1354-29del	NP_000243.1:n.1354-29del
XM_005274687.2:c.1354-29del	XP_005274744.1:n.1354-29del
XM_011531170.1:c.1420-29del	XP_011529472.1:n.1420-29del
XM_011531171.1:c.1399-29del	XP_011529473.1:n.1399-29del
XM_011531172.1:c.1399-29del	XP_011529474.1:n.1399-29del
XM_011531173.1:c.1354-29del	XP_011529475.1:n.1354-29del
XM_011531173.2:c.1354-29del	XP_011529475.1:n.1354-29del
XM_017029547.1:c.1399-29del	XP_016885036.1:n.1399-29del
XM_017029548.1:c.1399-29del	XP_016885037.1:n.1399-29del
XM_017029549.1:c.1354-29del	XP_016885038.1:n.1354-29del
XM_017029550.1:c.1243-29del	XP_016885039.1:n.1243-29del
XM_017029551.2:c.610-29del	XP_016885040.1:n.610-29del
NM_000252.3:c.1354-29del MANE Select	NP_000243.1:n.1354-29del
NM_001376906.1:c.1354-29del	NP_001363835.1:n.1354-29del
NM_001376907.1:c.1243-29del	NP_001363836.1:n.1243-29del
NM_001376908.1:c.1354-29del	NP_001363837.1:n.1354-29del