Canonical Allele Identifier: CA2182497198
Gene: TPM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.63066177T= , CM000677.2:g.63066177T= GRCh38
NC_000015.9:g.63358376T= , CM000677.1:g.63358376T= GRCh37
NC_000015.8:g.61145429T= NCBI36
NG_007557.1:g.28539T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000558868.6:n.1555+3532T=
ENST00000559831.6:c.*191+3532T= ENSP00000452977.2:n.*191+3532T=
ENST00000560615.6:c.394+3532T= ENSP00000453050.2:n.394+3532T=
ENST00000651622.2:c.*1026+92T= ENSP00000498540.2:n.*1026+92T=
ENST00000705544.1:c.728+92T=
ENST00000317516.12:c.664+3532T= ENSP00000322577.7:n.664+3532T=
ENST00000334895.10:c.664+3532T= ENSP00000334624.4:n.664+3532T=
ENST00000357980.9:c.898+3532T= ENSP00000350667.4:n.898+3532T=
ENST00000403994.9:c.*278T= MANE Select ENSP00000385107.4:n.*278T=
ENST00000404484.9:c.664+3532T= ENSP00000384315.4:n.664+3532T=
ENST00000559397.6:c.772+3532T= ENSP00000452879.1:n.772+3532T=
ENST00000644204.1:n.794+3532T=
ENST00000651344.1:n.1288+3532T=
ENST00000651577.1:c.394+3532T= ENSP00000498730.1:n.394+3532T=
ENST00000651590.1:c.*98+92T= ENSP00000498284.1:n.*98+92T=
ENST00000651704.1:c.394+3532T= ENSP00000498562.1:n.394+3532T=
ENST00000267996.11:c.772+3532T= ENSP00000267996.7:n.772+3532T=
ENST00000317516.11:c.664+3532T= ENSP00000322577.7:n.664+3532T=
ENST00000334895.9:c.664+3532T= ENSP00000334624.4:n.664+3532T=
ENST00000357980.8:c.898+3532T= ENSP00000350667.4:n.898+3532T=
ENST00000358278.7:c.772+3532T= ENSP00000351022.3:n.772+3532T=
ENST00000404484.8:c.664+3532T= ENSP00000384315.4:n.664+3532T=
ENST00000558072.5:n.291+3532T=
ENST00000558264.5:c.*191+3532T= ENSP00000452624.1:n.*191+3532T=
ENST00000558347.5:c.*180+3532T= ENSP00000452887.1:n.*180+3532T=
ENST00000558544.5:c.*380+3532T= ENSP00000453817.1:n.*380+3532T=
ENST00000559397.5:c.772+3532T= ENSP00000452879.1:n.772+3532T=
ENST00000559556.5:c.772+3532T= ENSP00000453941.1:n.772+3532T=
ENST00000560975.5:n.2621+3532T=
NM_001018004.1:c.772+3532T= NP_001018004.1:n.772+3532T=
NM_001018006.1:c.772+3532T= NP_001018006.1:n.772+3532T=
NM_001018007.1:c.772+3532T= NP_001018007.1:n.772+3532T=
NM_001018008.1:c.664+3532T= NP_001018008.1:n.664+3532T=
NM_001018020.1:c.772+3532T= NP_001018020.1:n.772+3532T=
NM_001301289.1:c.664+3532T= NP_001288218.1:n.664+3532T=
XM_005254637.1:c.898+3532T= XP_005254694.1:n.898+3532T=
XM_005254645.1:c.772+3532T= XP_005254702.1:n.772+3532T=
XM_005254652.1:c.664+3532T= XP_005254709.1:n.664+3532T=
XM_005254653.1:c.664+3532T= XP_005254710.1:n.664+3532T=
NM_001330344.1:c.664+3532T= NP_001317273.1:n.664+3532T=
NM_001330351.1:c.664+3532T= NP_001317280.1:n.664+3532T=
NM_001365776.1:c.772+3532T= NP_001352705.1:n.772+3532T=
NM_001365777.1:c.*190T= NP_001352706.1:n.*190T=
NM_001365778.1:c.898+3532T= NP_001352707.1:n.898+3532T=
NM_001365779.1:c.*326T= NP_001352708.1:n.*326T=
NM_001365780.1:c.*190T= NP_001352709.1:n.*190T=
NM_001365782.1:c.*2031T= NP_001352711.1:n.*2031T=
XM_017022539.2:c.772+3532T= XP_016878028.2:n.772+3532T=
XR_002957675.1:n.1730+3532T=
NM_000366.6:c.*326T= NP_000357.3:n.*326T=
NM_001018004.2:c.772+3532T= NP_001018004.1:n.772+3532T=
NM_001018005.2:c.*278T= MANE Select NP_001018005.1:n.*278T=
NM_001018006.2:c.772+3532T= NP_001018006.1:n.772+3532T=
NM_001018007.2:c.772+3532T= NP_001018007.1:n.772+3532T=
NM_001018008.2:c.664+3532T= NP_001018008.1:n.664+3532T=
NM_001018020.2:c.772+3532T= NP_001018020.1:n.772+3532T=
NM_001301244.2:c.*278T= NP_001288173.1:n.*278T=
NM_001301289.2:c.664+3532T= NP_001288218.1:n.664+3532T=
NM_001330344.2:c.664+3532T= NP_001317273.1:n.664+3532T=
NM_001330346.2:c.*278T= NP_001317275.1:n.*278T=
NM_001330351.2:c.664+3532T= NP_001317280.1:n.664+3532T=
NM_001365781.2:c.*2031T= NP_001352710.1:n.*2031T=