Canonical Allele Identifier: CA232695
Gene: TPM3 HGNC NCBI

Linked Data

ClinVar Variation Id: 42116
dbSNP Id: rs199474717

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154170454C>T , CM000663.2:g.154170454C>T GRCh38
NC_000001.10:g.154142930C>T , CM000663.1:g.154142930C>T GRCh37
NC_000001.9:g.152409554C>T NCBI36
NG_008621.1:g.26680G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000611659.5:c.547G>A ENSP00000480520.1:p.Glu183Lys
ENST00000312970.13:n.577G>A
ENST00000323144.12:c.610G>A ENSP00000357518.4:p.Glu204Lys
ENST00000328159.9:c.610G>A ENSP00000357520.1:p.Glu204Lys
ENST00000341372.8:c.*326G>A ENSP00000339378.4:n.*326G>A
ENST00000341485.10:c.610G>A ENSP00000341653.6:p.Glu204Lys
ENST00000368530.7:c.721G>A ENSP00000357516.3:p.Glu241Lys
ENST00000368533.8:c.610G>A ENSP00000357521.3:p.Glu204Lys
ENST00000651641.1:c.721G>A MANE Select ENSP00000498577.1:p.Glu241Lys
ENST00000651731.1:c.90G>A
ENST00000651873.1:c.631G>A
ENST00000271850.11:c.721G>A ENSP00000271850.7:p.Glu241Lys
ENST00000302206.9:c.340G>A ENSP00000307712.5:p.Glu114Lys
ENST00000312970.12:n.500G>A
ENST00000323144.11:c.610G>A ENSP00000357518.4:p.Glu204Lys
ENST00000328159.8:c.610G>A ENSP00000357520.1:p.Glu204Lys
ENST00000330188.13:c.610G>A ENSP00000339035.7:p.Glu204Lys
ENST00000341372.7:c.535G>A ENSP00000339378.3:p.Glu179Lys
ENST00000341485.9:c.562G>A ENSP00000341653.5:p.Glu188Lys
ENST00000368530.6:c.721G>A ENSP00000357516.2:p.Glu241Lys
ENST00000368531.6:c.610G>A ENSP00000357517.2:p.Glu204Lys
ENST00000368533.7:c.610G>A ENSP00000357521.3:p.Glu204Lys
ENST00000368545.7:n.728G>A
ENST00000469717.5:n.2624G>A
ENST00000504663.1:n.68G>A
ENST00000509409.5:c.*326G>A ENSP00000426521.1:n.*326G>A
ENST00000509601.1:c.*120G>A ENSP00000422207.1:n.*120G>A
ENST00000513769.5:n.295G>A
ENST00000611659.4:c.547G>A ENSP00000480520.1:p.Glu183Lys
NM_001043351.1:c.610G>A NP_001036816.1:p.Glu204Lys
NM_001043352.1:c.610G>A NP_001036817.1:p.Glu204Lys
NM_001043353.1:c.610G>A NP_001036818.1:p.Glu204Lys
NM_001278188.1:c.412G>A NP_001265117.1:p.Glu138Lys
NM_001278189.1:c.610G>A NP_001265118.1:p.Glu204Lys
NM_001278190.1:c.547G>A NP_001265119.1:p.Glu183Lys
NM_001278191.1:c.340G>A NP_001265120.1:p.Glu114Lys
NM_152263.3:c.721G>A NP_689476.2:p.Glu241Lys
NM_153649.3:c.610G>A NP_705935.1:p.Glu204Lys
NR_103461.1:n.736G>A
XM_006711515.1:c.721G>A XP_006711578.1:p.Glu241Lys
XM_006711517.1:c.721G>A XP_006711580.1:p.Glu241Lys
XM_006711518.1:c.721G>A XP_006711581.1:p.Glu241Lys
XM_006711519.1:c.721G>A XP_006711582.1:p.Glu241Lys
XM_006711520.1:c.721G>A XP_006711583.1:p.Glu241Lys
XM_006711521.1:c.721G>A XP_006711584.1:p.Glu241Lys
XM_006711522.2:c.610G>A XP_006711585.1:p.Glu204Lys
XM_006711523.2:c.610G>A XP_006711586.1:p.Glu204Lys
XM_011509950.1:c.721G>A XP_011508252.1:p.Glu241Lys
XM_011509951.1:c.721G>A XP_011508253.1:p.Glu241Lys
XM_011509952.1:c.610G>A XP_011508254.1:p.Glu204Lys
XM_011509953.1:c.610G>A XP_011508255.1:p.Glu204Lys
XM_011509954.1:c.610G>A XP_011508256.1:p.Glu204Lys
NM_001349679.1:c.610G>A NP_001336608.1:p.Glu204Lys
NM_001364679.1:c.721G>A NP_001351608.1:p.Glu241Lys
NM_001364680.1:c.721G>A NP_001351609.1:p.Glu241Lys
NM_001364681.1:c.721G>A NP_001351610.1:p.Glu241Lys
NM_001364682.1:c.721G>A NP_001351611.1:p.Glu241Lys
NM_001364683.1:c.610G>A NP_001351612.1:p.Glu204Lys
NM_152263.4:c.721G>A MANE Select NP_689476.2:p.Glu241Lys
NM_001043351.2:c.610G>A NP_001036816.1:p.Glu204Lys
NM_001043352.2:c.610G>A NP_001036817.1:p.Glu204Lys
NM_001043353.2:c.610G>A NP_001036818.1:p.Glu204Lys
NM_001278188.2:c.412G>A NP_001265117.1:p.Glu138Lys
NM_001278189.2:c.610G>A NP_001265118.1:p.Glu204Lys
NM_001278191.2:c.340G>A NP_001265120.1:p.Glu114Lys
NM_001349679.2:c.610G>A NP_001336608.1:p.Glu204Lys
NM_001364679.2:c.721G>A NP_001351608.1:p.Glu241Lys
NM_001364680.2:c.721G>A NP_001351609.1:p.Glu241Lys
NM_001364681.2:c.721G>A NP_001351610.1:p.Glu241Lys
NM_153649.4:c.610G>A NP_705935.1:p.Glu204Lys
NR_103461.2:n.705G>A
NM_001278190.2:c.547G>A NP_001265119.1:p.Glu183Lys