Canonical Allele Identifier: CA2182497170
Gene: TPM1 HGNC NCBI

Linked Data

dbSNP Id: rs1595686768

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.63066106A>G , CM000677.2:g.63066106A>G GRCh38
NC_000015.9:g.63358305A>G , CM000677.1:g.63358305A>G GRCh37
NC_000015.8:g.61145358A>G NCBI36
NG_007557.1:g.28468A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000558868.6:n.1555+3461A>G
ENST00000559831.6:c.*191+3461A>G ENSP00000452977.2:n.*191+3461A>G
ENST00000560615.6:c.394+3461A>G ENSP00000453050.2:n.394+3461A>G
ENST00000651622.2:c.*1026+21A>G ENSP00000498540.2:n.*1026+21A>G
ENST00000705544.1:c.728+21A>G
ENST00000317516.12:c.664+3461A>G ENSP00000322577.7:n.664+3461A>G
ENST00000334895.10:c.664+3461A>G ENSP00000334624.4:n.664+3461A>G
ENST00000357980.9:c.898+3461A>G ENSP00000350667.4:n.898+3461A>G
ENST00000403994.9:c.*207A>G MANE Select ENSP00000385107.4:n.*207A>G
ENST00000404484.9:c.664+3461A>G ENSP00000384315.4:n.664+3461A>G
ENST00000559397.6:c.772+3461A>G ENSP00000452879.1:n.772+3461A>G
ENST00000644204.1:n.794+3461A>G
ENST00000651344.1:n.1288+3461A>G
ENST00000651577.1:c.394+3461A>G ENSP00000498730.1:n.394+3461A>G
ENST00000651590.1:c.*98+21A>G ENSP00000498284.1:n.*98+21A>G
ENST00000651704.1:c.394+3461A>G ENSP00000498562.1:n.394+3461A>G
ENST00000267996.11:c.772+3461A>G ENSP00000267996.7:n.772+3461A>G
ENST00000317516.11:c.664+3461A>G ENSP00000322577.7:n.664+3461A>G
ENST00000334895.9:c.664+3461A>G ENSP00000334624.4:n.664+3461A>G
ENST00000357980.8:c.898+3461A>G ENSP00000350667.4:n.898+3461A>G
ENST00000358278.7:c.772+3461A>G ENSP00000351022.3:n.772+3461A>G
ENST00000404484.8:c.664+3461A>G ENSP00000384315.4:n.664+3461A>G
ENST00000558072.5:n.291+3461A>G
ENST00000558264.5:c.*191+3461A>G ENSP00000452624.1:n.*191+3461A>G
ENST00000558347.5:c.*180+3461A>G ENSP00000452887.1:n.*180+3461A>G
ENST00000558544.5:c.*380+3461A>G ENSP00000453817.1:n.*380+3461A>G
ENST00000559397.5:c.772+3461A>G ENSP00000452879.1:n.772+3461A>G
ENST00000559556.5:c.772+3461A>G ENSP00000453941.1:n.772+3461A>G
ENST00000560445.1:c.*119A>G ENSP00000452999.1:n.*119A>G
ENST00000560975.5:n.2621+3461A>G
NM_001018004.1:c.772+3461A>G NP_001018004.1:n.772+3461A>G
NM_001018006.1:c.772+3461A>G NP_001018006.1:n.772+3461A>G
NM_001018007.1:c.772+3461A>G NP_001018007.1:n.772+3461A>G
NM_001018008.1:c.664+3461A>G NP_001018008.1:n.664+3461A>G
NM_001018020.1:c.772+3461A>G NP_001018020.1:n.772+3461A>G
NM_001301289.1:c.664+3461A>G NP_001288218.1:n.664+3461A>G
XM_005254637.1:c.898+3461A>G XP_005254694.1:n.898+3461A>G
XM_005254638.2:c.*119A>G XP_005254695.1:n.*119A>G
XM_005254639.2:c.*119A>G XP_005254696.1:n.*119A>G
XM_005254640.2:c.*119A>G XP_005254697.1:n.*119A>G
XM_005254641.2:c.*119A>G XP_005254698.1:n.*119A>G
XM_005254645.1:c.772+3461A>G XP_005254702.1:n.772+3461A>G
XM_005254647.2:c.*119A>G XP_005254704.1:n.*119A>G
XM_005254650.2:c.*207A>G XP_005254707.1:n.*207A>G
XM_005254652.1:c.664+3461A>G XP_005254709.1:n.664+3461A>G
XM_005254653.1:c.664+3461A>G XP_005254710.1:n.664+3461A>G
XM_006720667.2:c.*207A>G XP_006720730.1:n.*207A>G
XM_006720669.2:c.*119A>G XP_006720732.1:n.*119A>G
NM_001330344.1:c.664+3461A>G NP_001317273.1:n.664+3461A>G
NM_001330351.1:c.664+3461A>G NP_001317280.1:n.664+3461A>G
NM_001365776.1:c.772+3461A>G NP_001352705.1:n.772+3461A>G
NM_001365777.1:c.*119A>G NP_001352706.1:n.*119A>G
NM_001365778.1:c.898+3461A>G NP_001352707.1:n.898+3461A>G
NM_001365779.1:c.*255A>G NP_001352708.1:n.*255A>G
NM_001365780.1:c.*119A>G NP_001352709.1:n.*119A>G
NM_001365782.1:c.*1960A>G NP_001352711.1:n.*1960A>G
XM_017022539.2:c.772+3461A>G XP_016878028.2:n.772+3461A>G
XR_002957675.1:n.1730+3461A>G
NM_000366.6:c.*255A>G NP_000357.3:n.*255A>G
NM_001018004.2:c.772+3461A>G NP_001018004.1:n.772+3461A>G
NM_001018005.2:c.*207A>G MANE Select NP_001018005.1:n.*207A>G
NM_001018006.2:c.772+3461A>G NP_001018006.1:n.772+3461A>G
NM_001018007.2:c.772+3461A>G NP_001018007.1:n.772+3461A>G
NM_001018008.2:c.664+3461A>G NP_001018008.1:n.664+3461A>G
NM_001018020.2:c.772+3461A>G NP_001018020.1:n.772+3461A>G
NM_001301244.2:c.*207A>G NP_001288173.1:n.*207A>G
NM_001301289.2:c.664+3461A>G NP_001288218.1:n.664+3461A>G
NM_001330344.2:c.664+3461A>G NP_001317273.1:n.664+3461A>G
NM_001330346.2:c.*207A>G NP_001317275.1:n.*207A>G
NM_001330351.2:c.664+3461A>G NP_001317280.1:n.664+3461A>G
NM_001365781.2:c.*1960A>G NP_001352710.1:n.*1960A>G