Canonical Allele Identifier: CA30766304
Gene: TPM3 HGNC NCBI

Linked Data

dbSNP Id: rs121964851

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154167938_154167940del , CM000663.2:g.154167938_154167940del GRCh38
NC_000001.10:g.154140414_154140416del , CM000663.1:g.154140414_154140416del GRCh37
NC_000001.9:g.152407038_152407040del NCBI36
NG_008621.1:g.29196_29198del

Transcript Alleles

HGVS Amino-acid change
ENST00000611659.5:c.601+2462_601+2464del ENSP00000480520.1:n.601+2462_601+2464del
ENST00000312970.13:n.631+2462_631+2464del
ENST00000323144.12:c.664+2462_664+2464del ENSP00000357518.4:n.664+2462_664+2464del
ENST00000328159.9:c.743+1367_743+1369del ENSP00000357520.1:n.743+1367_743+1369del
ENST00000341372.8:c.*380+2462_*380+2464del ENSP00000339378.4:n.*380+2462_*380+2464de...
ENST00000341485.10:c.664+2462_664+2464del ENSP00000341653.6:n.664+2462_664+2464del
ENST00000368530.7:c.857_*1del ENSP00000357516.3:n.[c.857_*1del;Ter286Le...
ENST00000368533.8:c.664+2462_664+2464del ENSP00000357521.3:n.664+2462_664+2464del
ENST00000651641.1:c.857_*1del MANE Select ENSP00000498577.1:n.[c.857_*1del;Ter286Le...
ENST00000651731.1:c.223+1367_223+1369del
ENST00000651873.1:c.685+2462_685+2464del
ENST00000271850.11:c.775+2462_775+2464del ENSP00000271850.7:n.775+2462_775+2464del
ENST00000302206.9:c.394+2462_394+2464del ENSP00000307712.5:n.394+2462_394+2464del
ENST00000312970.12:n.554+2462_554+2464del
ENST00000323144.11:c.664+2462_664+2464del ENSP00000357518.4:n.664+2462_664+2464del
ENST00000328159.8:c.743+1367_743+1369del ENSP00000357520.1:n.743+1367_743+1369del
ENST00000330188.13:c.664+2462_664+2464del ENSP00000339035.7:n.664+2462_664+2464del
ENST00000341372.7:c.589+2462_589+2464del ENSP00000339378.3:n.589+2462_589+2464del
ENST00000341485.9:c.616+2462_616+2464del ENSP00000341653.5:n.616+2462_616+2464del
ENST00000368530.6:c.857_*1del ENSP00000357516.2:n.[c.857_*1del;Ter286Le...
ENST00000368531.6:c.664+2462_664+2464del ENSP00000357517.2:n.664+2462_664+2464del
ENST00000368533.7:c.664+2462_664+2464del ENSP00000357521.3:n.664+2462_664+2464del
ENST00000368545.7:n.782+2462_782+2464del
ENST00000469717.5:n.2678+2462_2678+2464del
ENST00000509409.5:c.*380+2462_*380+2464del ENSP00000426521.1:n.*380+2462_*380+2464de...
ENST00000513769.5:n.349+2462_349+2464del
ENST00000611659.4:c.601+2462_601+2464del ENSP00000480520.1:n.601+2462_601+2464del
NM_001043351.1:c.664+2462_664+2464del NP_001036816.1:n.664+2462_664+2464del
NM_001043352.1:c.664+2462_664+2464del NP_001036817.1:n.664+2462_664+2464del
NM_001043353.1:c.664+2462_664+2464del NP_001036818.1:n.664+2462_664+2464del
NM_001278188.1:c.466+2462_466+2464del NP_001265117.1:n.466+2462_466+2464del
NM_001278189.1:c.743+1367_743+1369del NP_001265118.1:n.743+1367_743+1369del
NM_001278190.1:c.601+2462_601+2464del NP_001265119.1:n.601+2462_601+2464del
NM_001278191.1:c.394+2462_394+2464del NP_001265120.1:n.394+2462_394+2464del
NM_152263.3:c.857_*1del NP_689476.2:n.[c.857_*1del;Ter286LeuextTe...
NM_153649.3:c.664+2462_664+2464del NP_705935.1:n.664+2462_664+2464del
NR_103461.1:n.790+2462_790+2464del
XM_006711515.1:c.775+2462_775+2464del XP_006711578.1:n.775+2462_775+2464del
XM_006711517.1:c.857_*1del XP_006711580.1:n.[c.857_*1del;Ter286Leuex...
XM_006711518.1:c.854+1367_854+1369del XP_006711581.1:n.854+1367_854+1369del
XM_006711519.1:c.775+2462_775+2464del XP_006711582.1:n.775+2462_775+2464del
XM_006711520.1:c.775+2462_775+2464del XP_006711583.1:n.775+2462_775+2464del
XM_006711521.1:c.775+2462_775+2464del XP_006711584.1:n.775+2462_775+2464del
XM_006711522.2:c.746_*1del XP_006711585.1:n.[c.746_*1del;Ter249Leuex...
XM_011509950.1:c.854+1367_854+1369del XP_011508252.1:n.854+1367_854+1369del
XM_011509951.1:c.854+1367_854+1369del XP_011508253.1:n.854+1367_854+1369del
XM_011509952.1:c.743+1367_743+1369del XP_011508254.1:n.743+1367_743+1369del
XM_011509953.1:c.743+1367_743+1369del XP_011508255.1:n.743+1367_743+1369del
NM_001349679.1:c.743+1367_743+1369del NP_001336608.1:n.743+1367_743+1369del
NM_001364679.1:c.775+2462_775+2464del NP_001351608.1:n.775+2462_775+2464del
NM_001364680.1:c.775+2462_775+2464del NP_001351609.1:n.775+2462_775+2464del
NM_001364681.1:c.775+2462_775+2464del NP_001351610.1:n.775+2462_775+2464del
NM_001364682.1:c.857_*1del NP_001351611.1:n.[c.857_*1del;Ter286Leuex...
NM_001364683.1:c.746_*1del NP_001351612.1:n.[c.746_*1del;Ter249Leuex...
NM_152263.4:c.857_*1del MANE Select NP_689476.2:n.[c.857_*1del;Ter286LeuextTe...
NM_001043351.2:c.664+2462_664+2464del NP_001036816.1:n.664+2462_664+2464del
NM_001043352.2:c.664+2462_664+2464del NP_001036817.1:n.664+2462_664+2464del
NM_001043353.2:c.664+2462_664+2464del NP_001036818.1:n.664+2462_664+2464del
NM_001278188.2:c.466+2462_466+2464del NP_001265117.1:n.466+2462_466+2464del
NM_001278189.2:c.743+1367_743+1369del NP_001265118.1:n.743+1367_743+1369del
NM_001278191.2:c.394+2462_394+2464del NP_001265120.1:n.394+2462_394+2464del
NM_001349679.2:c.743+1367_743+1369del NP_001336608.1:n.743+1367_743+1369del
NM_001364679.2:c.775+2462_775+2464del NP_001351608.1:n.775+2462_775+2464del
NM_001364680.2:c.775+2462_775+2464del NP_001351609.1:n.775+2462_775+2464del
NM_001364681.2:c.775+2462_775+2464del NP_001351610.1:n.775+2462_775+2464del
NM_153649.4:c.664+2462_664+2464del NP_705935.1:n.664+2462_664+2464del
NR_103461.2:n.759+2462_759+2464del
NM_001278190.2:c.601+2462_601+2464del NP_001265119.1:n.601+2462_601+2464del