Canonical Allele Identifier: CA2518985619
Gene: TPM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154164140del , CM000663.2:g.154164140del GRCh38
NC_000001.10:g.154136616del , CM000663.1:g.154136616del GRCh37
NC_000001.9:g.152403240del NCBI36
NG_008621.1:g.32994del

Transcript Alleles

HGVS Amino-acid Change
NM_152263.4:c.*3797del MANE Select NP_689476.2:n.*3797del
ENST00000651641.1:c.*3797del MANE Select ENSP00000498577.1:n.*3797del
NM_001043351.1:c.664+6260del NP_001036816.1:n.664+6260del
NM_001043351.2:c.664+6260del NP_001036816.1:n.664+6260del
NM_001043352.1:c.665-5092del NP_001036817.1:n.665-5092del
NM_001043352.2:c.665-5092del NP_001036817.1:n.665-5092del
NM_001043353.1:c.665-5092del NP_001036818.1:n.665-5092del
NM_001043353.2:c.665-5092del NP_001036818.1:n.665-5092del
NM_001278188.1:c.466+6260del NP_001265117.1:n.466+6260del
NM_001278188.2:c.466+6260del NP_001265117.1:n.466+6260del
NM_001278189.1:c.743+5165del NP_001265118.1:n.743+5165del
NM_001278189.2:c.743+5165del NP_001265118.1:n.743+5165del
NM_001278190.1:c.601+6260del NP_001265119.1:n.601+6260del
NM_001278190.2:c.601+6260del NP_001265119.1:n.601+6260del
NM_001278191.1:c.394+6260del NP_001265120.1:n.394+6260del
NM_001278191.2:c.394+6260del NP_001265120.1:n.394+6260del
NM_001349679.1:c.743+5165del NP_001336608.1:n.743+5165del
NM_001349679.2:c.743+5165del NP_001336608.1:n.743+5165del
NM_001364679.1:c.775+6260del NP_001351608.1:n.775+6260del
NM_001364679.2:c.775+6260del NP_001351608.1:n.775+6260del
NM_001364680.1:c.775+6260del NP_001351609.1:n.775+6260del
NM_001364680.2:c.775+6260del NP_001351609.1:n.775+6260del
NM_001364681.1:c.776-5092del NP_001351610.1:n.776-5092del
NM_001364681.2:c.776-5092del NP_001351610.1:n.776-5092del
NM_001364682.1:c.*3797del NP_001351611.1:n.*3797del
NM_001364683.1:c.*3797del NP_001351612.1:n.*3797del
NM_152263.3:c.*3797del NP_689476.2:n.*3797del
NM_153649.3:c.664+6260del NP_705935.1:n.664+6260del
NM_153649.4:c.664+6260del NP_705935.1:n.664+6260del
NR_103461.1:n.790+6260del
NR_103461.2:n.759+6260del
ENST00000271850.11:c.775+6260del ENSP00000271850.7:n.775+6260del
ENST00000302206.9:c.394+6260del ENSP00000307712.5:n.394+6260del
ENST00000312970.12:n.554+6260del
ENST00000312970.13:n.631+6260del
ENST00000323144.11:c.665-5092del ENSP00000357518.4:n.665-5092del
ENST00000323144.12:c.665-5092del ENSP00000357518.4:n.665-5092del
ENST00000328159.8:c.743+5165del ENSP00000357520.1:n.743+5165del
ENST00000328159.9:c.743+5165del ENSP00000357520.1:n.743+5165del
ENST00000330188.13:c.664+6260del ENSP00000339035.7:n.664+6260del
ENST00000341372.7:c.589+6260del ENSP00000339378.3:n.589+6260del
ENST00000341372.8:c.*380+6260del ENSP00000339378.4:n.*380+6260del
ENST00000341485.10:c.665-5092del ENSP00000341653.6:n.665-5092del
ENST00000341485.9:c.616+6260del ENSP00000341653.5:n.616+6260del
ENST00000368531.6:c.665-5092del ENSP00000357517.2:n.665-5092del
ENST00000368533.7:c.664+6260del ENSP00000357521.3:n.664+6260del
ENST00000368533.8:c.664+6260del ENSP00000357521.3:n.664+6260del
ENST00000368545.7:n.782+6260del
ENST00000469717.5:n.2678+6260del
ENST00000509409.5:c.*380+6260del ENSP00000426521.1:n.*380+6260del
ENST00000513769.5:n.349+6260del
ENST00000611659.4:c.601+6260del ENSP00000480520.1:n.601+6260del
ENST00000611659.5:c.601+6260del ENSP00000480520.1:n.601+6260del
ENST00000651731.1:c.224-2362del
ENST00000651873.1:c.685+6260del
XM_006711515.1:c.775+6260del XP_006711578.1:n.775+6260del
XM_006711518.1:c.854+5165del XP_006711581.1:n.854+5165del
XM_006711519.1:c.775+6260del XP_006711582.1:n.775+6260del
XM_006711520.1:c.776-5092del XP_006711583.1:n.776-5092del
XM_006711521.1:c.776-5092del XP_006711584.1:n.776-5092del
XM_011509950.1:c.855-5092del XP_011508252.1:n.855-5092del
XM_011509951.1:c.855-5092del XP_011508253.1:n.855-5092del
XM_011509952.1:c.744-5092del XP_011508254.1:n.744-5092del
XM_011509953.1:c.744-5092del XP_011508255.1:n.744-5092del