Canonical Allele Identifier: CA2465385871
Gene: MTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.150658017A= , CM000685.2:g.150658017A= GRCh38
NC_000023.10:g.149826490A= , CM000685.1:g.149826490A= GRCh37
NC_000023.9:g.149577148A= NCBI36
NG_008199.1:g.94444A= , LRG_839:g.94444A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684910.1:c.*783A= ENSP00000509844.1:n.*783A=
ENST00000685439.1:c.905A= ENSP00000508454.1:p.Lys302=
ENST00000685944.1:c.1250A= ENSP00000509266.1:p.Lys417=
ENST00000686212.1:n.852A=
ENST00000687215.1:c.*1005A= ENSP00000509706.1:n.*1005A=
ENST00000688152.1:c.*694A= ENSP00000509360.1:n.*694A=
ENST00000688403.1:c.506A= ENSP00000508944.1:p.Lys169=
ENST00000689314.1:c.1295A= ENSP00000510607.1:p.Lys432=
ENST00000689694.1:c.1250A= ENSP00000508718.1:p.Lys417=
ENST00000689810.1:c.*899A= ENSP00000510635.1:n.*899A=
ENST00000690282.1:c.506A= ENSP00000509809.1:p.Lys169=
ENST00000690351.1:c.*902A= ENSP00000509728.1:n.*902A=
ENST00000691232.1:c.905A= ENSP00000509675.1:p.Lys302=
ENST00000691482.1:n.2265A=
ENST00000691686.1:c.1250A= ENSP00000509784.1:p.Lys417=
ENST00000691851.1:c.1053+8116A= ENSP00000510106.1:n.1053+8116A=
ENST00000692015.1:c.1037A= ENSP00000510634.1:p.Lys346=
ENST00000692638.1:c.*1055A= ENSP00000509412.1:n.*1055A=
ENST00000692852.1:c.1061A= ENSP00000510337.1:p.Lys354=
ENST00000692915.1:c.*1396A= ENSP00000508547.1:n.*1396A=
ENST00000370396.7:c.1250A= MANE Select ENSP00000359423.3:p.Lys417=
ENST00000306167.11:n.1117A=
ENST00000370396.6:c.1250A= ENSP00000359423.2:p.Lys417=
NM_000252.2:c.1250A= , LRG_839t1:c.1250A= NP_000243.1:p.Lys417=
XM_005274687.2:c.1250A= XP_005274744.1:p.Lys417=
XM_011531170.1:c.1316A= XP_011529472.1:p.Lys439=
XM_011531171.1:c.1295A= XP_011529473.1:p.Lys432=
XM_011531172.1:c.1295A= XP_011529474.1:p.Lys432=
XM_011531173.1:c.1250A= XP_011529475.1:p.Lys417=
XM_011531173.2:c.1250A= XP_011529475.1:p.Lys417=
XM_017029547.1:c.1295A= XP_016885036.1:p.Lys432=
XM_017029548.1:c.1295A= XP_016885037.1:p.Lys432=
XM_017029549.1:c.1250A= XP_016885038.1:p.Lys417=
XM_017029550.1:c.1139A= XP_016885039.1:p.Lys380=
XM_017029551.2:c.506A= XP_016885040.1:p.Lys169=
NM_000252.3:c.1250A= MANE Select NP_000243.1:p.Lys417=
NM_001376906.1:c.1250A= NP_001363835.1:p.Lys417=
NM_001376907.1:c.1139A= NP_001363836.1:p.Lys380=
NM_001376908.1:c.1250A= NP_001363837.1:p.Lys417=