Canonical Allele Identifier: CA1139655520

Gene: TPM3

Linked Data

• ClinVar Variation Id: 974884
• ClinVar RCV Id: RCV001251175

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154169979_154175253del , CM000663.2:g.154169979_154175253del	GRCh38
NC_000001.10:g.154142455_154147729del , CM000663.1:g.154142455_154147729del	GRCh37
NC_000001.9:g.152409079_152414353del	NCBI36
NG_008621.1:g.21882_27156del

Transcript Alleles

HGVS	Amino-acid change
ENST00000611659.5:c.266+863_601+422del
ENST00000312970.13:n.233+863_631+422del
ENST00000323144.12:c.266+863_664+422del
ENST00000328159.9:c.266+863_664+422del
ENST00000341372.8:c.133-2051_*380+422del
ENST00000341485.10:c.266+863_664+422del
ENST00000368530.7:c.377+863_775+422del
ENST00000368533.8:c.266+863_664+422del
ENST00000651641.1:c.377+863_775+422del
ENST00000651873.1:c.189+863_685+422del
ENST00000271850.11:c.377+863_775+422del
ENST00000302206.9:c.-5+863_394+422del
ENST00000312970.12:n.156+863_554+422del
ENST00000323144.11:c.266+863_664+422del
ENST00000328159.8:c.266+863_664+422del
ENST00000330188.13:c.266+863_664+422del
ENST00000341372.7:c.191+863_589+422del
ENST00000341485.9:c.253+876_616+422del
ENST00000368530.6:c.377+863_775+422del
ENST00000368531.6:c.266+863_664+422del
ENST00000368533.7:c.266+863_664+422del
ENST00000469717.5:n.161-2051_2678+422del
ENST00000509409.5:c.133-2051_*380+422del
ENST00000611659.4:c.266+863_601+422del
NM_001043351.1:c.266+863_664+422del
NM_001043352.1:c.266+863_664+422del
NM_001043353.1:c.266+863_664+422del
NM_001278188.1:c.69-2051_466+422del
NM_001278189.1:c.266+863_664+422del
NM_001278190.1:c.266+863_601+422del
NM_001278191.1:c.-5+863_394+422del
NM_152263.3:c.377+863_775+422del
NM_153649.3:c.266+863_664+422del
NR_103461.1:n.396+863_790+422del
XM_006711515.1:c.377+863_775+422del
XM_006711517.1:c.377+863_775+422del
XM_006711518.1:c.377+863_775+422del
XM_006711519.1:c.377+863_775+422del
XM_006711520.1:c.377+863_775+422del
XM_006711521.1:c.377+863_775+422del
XM_006711522.2:c.266+863_664+422del
XM_006711523.2:c.266+863_664+422del
XM_011509950.1:c.377+863_775+422del
XM_011509951.1:c.377+863_775+422del
XM_011509952.1:c.266+863_664+422del
XM_011509953.1:c.266+863_664+422del
XM_011509954.1:c.266+863_664+422del
NM_001349679.1:c.266+863_664+422del
NM_001364679.1:c.377+863_775+422del
NM_001364680.1:c.377+863_775+422del
NM_001364681.1:c.377+863_775+422del
NM_001364682.1:c.377+863_775+422del
NM_001364683.1:c.266+863_664+422del
NM_152263.4:c.377+863_775+422del
NM_001043351.2:c.266+863_664+422del
NM_001043352.2:c.266+863_664+422del
NM_001043353.2:c.266+863_664+422del
NM_001278188.2:c.69-2051_466+422del
NM_001278189.2:c.266+863_664+422del
NM_001278191.2:c.-5+863_394+422del
NM_001349679.2:c.266+863_664+422del
NM_001364679.2:c.377+863_775+422del
NM_001364680.2:c.377+863_775+422del
NM_001364681.2:c.377+863_775+422del
NM_153649.4:c.266+863_664+422del
NR_103461.2:n.365+863_759+422del
NM_001278190.2:c.266+863_601+422del