Canonical Allele Identifier: CA2480754961
Gene: TPM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154173155T= , CM000663.2:g.154173155T= GRCh38
NC_000001.10:g.154145631T= , CM000663.1:g.154145631T= GRCh37
NC_000001.9:g.152412255T= NCBI36
NG_008621.1:g.23979A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000611659.5:c.313A= ENSP00000480520.1:p.Met105=
ENST00000312970.13:n.280A=
ENST00000323144.12:c.313A= ENSP00000357518.4:p.Met105=
ENST00000328159.9:c.313A= ENSP00000357520.1:p.Met105=
ENST00000341372.8:c.*29A= ENSP00000339378.4:n.*29A=
ENST00000341485.10:c.313A= ENSP00000341653.6:p.Met105=
ENST00000368530.7:c.424A= ENSP00000357516.3:p.Met142=
ENST00000368533.8:c.313A= ENSP00000357521.3:p.Met105=
ENST00000651641.1:c.424A= MANE Select ENSP00000498577.1:p.Met142=
ENST00000651644.1:c.424A= ENSP00000498648.1:p.Met142=
ENST00000651873.1:c.334A=
ENST00000271850.11:c.424A= ENSP00000271850.7:p.Met142=
ENST00000302206.9:c.43A= ENSP00000307712.5:p.Met15=
ENST00000312970.12:n.203A=
ENST00000323144.11:c.313A= ENSP00000357518.4:p.Met105=
ENST00000328159.8:c.313A= ENSP00000357520.1:p.Met105=
ENST00000330188.13:c.313A= ENSP00000339035.7:p.Met105=
ENST00000341372.7:c.238A= ENSP00000339378.3:p.Met80=
ENST00000341485.9:c.265A= ENSP00000341653.5:p.Met89=
ENST00000368527.7:n.389A=
ENST00000368530.6:c.424A= ENSP00000357516.2:p.Met142=
ENST00000368531.6:c.313A= ENSP00000357517.2:p.Met105=
ENST00000368533.7:c.313A= ENSP00000357521.3:p.Met105=
ENST00000469717.5:n.207A=
ENST00000473036.2:n.368A=
ENST00000505010.5:n.175A=
ENST00000509409.5:c.*29A= ENSP00000426521.1:n.*29A=
ENST00000509601.1:c.267-1064A= ENSP00000422207.1:n.267-1064A=
ENST00000611659.4:c.313A= ENSP00000480520.1:p.Met105=
NM_001043351.1:c.313A= NP_001036816.1:p.Met105=
NM_001043352.1:c.313A= NP_001036817.1:p.Met105=
NM_001043353.1:c.313A= NP_001036818.1:p.Met105=
NM_001278188.1:c.115A= NP_001265117.1:p.Met39=
NM_001278189.1:c.313A= NP_001265118.1:p.Met105=
NM_001278190.1:c.313A= NP_001265119.1:p.Met105=
NM_001278191.1:c.43A= NP_001265120.1:p.Met15=
NM_152263.3:c.424A= NP_689476.2:p.Met142=
NM_153649.3:c.313A= NP_705935.1:p.Met105=
NR_103461.1:n.443A=
XM_006711515.1:c.424A= XP_006711578.1:p.Met142=
XM_006711517.1:c.424A= XP_006711580.1:p.Met142=
XM_006711518.1:c.424A= XP_006711581.1:p.Met142=
XM_006711519.1:c.424A= XP_006711582.1:p.Met142=
XM_006711520.1:c.424A= XP_006711583.1:p.Met142=
XM_006711521.1:c.424A= XP_006711584.1:p.Met142=
XM_006711522.2:c.313A= XP_006711585.1:p.Met105=
XM_006711523.2:c.313A= XP_006711586.1:p.Met105=
XM_011509950.1:c.424A= XP_011508252.1:p.Met142=
XM_011509951.1:c.424A= XP_011508253.1:p.Met142=
XM_011509952.1:c.313A= XP_011508254.1:p.Met105=
XM_011509953.1:c.313A= XP_011508255.1:p.Met105=
XM_011509954.1:c.313A= XP_011508256.1:p.Met105=
NM_001349679.1:c.313A= NP_001336608.1:p.Met105=
NM_001364679.1:c.424A= NP_001351608.1:p.Met142=
NM_001364680.1:c.424A= NP_001351609.1:p.Met142=
NM_001364681.1:c.424A= NP_001351610.1:p.Met142=
NM_001364682.1:c.424A= NP_001351611.1:p.Met142=
NM_001364683.1:c.313A= NP_001351612.1:p.Met105=
NM_152263.4:c.424A= MANE Select NP_689476.2:p.Met142=
NM_001043351.2:c.313A= NP_001036816.1:p.Met105=
NM_001043352.2:c.313A= NP_001036817.1:p.Met105=
NM_001043353.2:c.313A= NP_001036818.1:p.Met105=
NM_001278188.2:c.115A= NP_001265117.1:p.Met39=
NM_001278189.2:c.313A= NP_001265118.1:p.Met105=
NM_001278191.2:c.43A= NP_001265120.1:p.Met15=
NM_001349679.2:c.313A= NP_001336608.1:p.Met105=
NM_001364679.2:c.424A= NP_001351608.1:p.Met142=
NM_001364680.2:c.424A= NP_001351609.1:p.Met142=
NM_001364681.2:c.424A= NP_001351610.1:p.Met142=
NM_153649.4:c.313A= NP_705935.1:p.Met105=
NR_103461.2:n.412A=
NM_001278190.2:c.313A= NP_001265119.1:p.Met105=