Canonical Allele Identifier: CA018039
Gene: TPM1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 31888
dbSNP Id: rs1071646

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.63059641C>A , CM000677.2:g.63059641C>A GRCh38
NC_000015.8:g.61138893C>A NCBI36
NC_000015.9:g.63351840C>A , CM000677.1:g.63351840C>A GRCh37
NG_007557.1:g.22003C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000267996.11:c.453C>A ENSP00000267996.7:p.Ala151=
ENST00000288398.10:c.453C>A ENSP00000288398.6:p.Ala151=
ENST00000317516.11:n.345C>A ENSP00000322577.7:p.Ala115=
ENST00000334895.9:c.345C>A ENSP00000334624.4:p.Ala115=
ENST00000357980.8:c.579C>A ENSP00000350667.4:p.Ala193=
ENST00000358278.7:c.453C>A ENSP00000351022.3:p.Ala151=
ENST00000403994.7:c.453C>A ENSP00000385107.3:p.Ala151=
ENST00000404484.8:c.345C>A ENSP00000384315.4:p.Ala115=
ENST00000558264.5:c.75C>A ENSP00000452624.1:p.Ala25=
ENST00000558314.5:n.853C>A
ENST00000558347.5:c.375-1228C>A ENSP00000452887.1:p.=
ENST00000558400.1:n.337C>A
ENST00000558544.5:c.*61C>A ENSP00000453817.1:p.=
ENST00000558868.5:n.384C>A
ENST00000559281.5:n.345C>A ENSP00000452658.1:p.Ala115=
ENST00000559397.5:c.453C>A ENSP00000452879.1:p.Ala151=
ENST00000559556.5:c.453C>A ENSP00000453941.1:p.Ala151=
ENST00000559831.5:n.225C>A ENSP00000452977.1:p.Ala75=
ENST00000560445.1:c.187-6320C>A ENSP00000452999.1:p.=
ENST00000560615.5:c.75C>A ENSP00000453050.1:p.Ala25=
ENST00000560959.5:c.345C>A ENSP00000453724.1:p.Ala115=
ENST00000560970.5:n.395C>A
ENST00000560975.5:n.1361C>A
ENST00000561266.5:n.269C>A
ENST00000561395.5:n.189+3C>A ENSP00000453092.1:p.=
NM_000366.5:c.453C>A VV NP_000357.3:p.Ala151=
NM_001018004.1:c.453C>A VV NP_001018004.1:p.Ala151=
NM_001018005.1:c.453C>A VV NP_001018005.1:p.Ala151=
NM_001018006.1:c.453C>A VV NP_001018006.1:p.Ala151=
NM_001018007.1:c.453C>A VV NP_001018007.1:p.Ala151=
NM_001018008.1:c.345C>A VV NP_001018008.1:p.Ala115=
NM_001018020.1:c.453C>A VV NP_001018020.1:p.Ala151=
NM_001301244.1:c.453C>A VV NP_001288173.1:p.Ala151=
NM_001301289.1:c.345C>A VV NP_001288218.1:p.Ala115=
XM_005254637.1:c.579C>A XP_005254694.1:p.Ala193=
XM_005254638.2:c.453C>A XP_005254695.1:p.Ala151=
XM_005254639.2:c.453C>A XP_005254696.1:p.Ala151=
XM_005254640.2:c.453C>A XP_005254697.1:p.Ala151=
XM_005254641.2:c.453C>A XP_005254698.1:p.Ala151=
XM_005254645.1:c.453C>A XP_005254702.1:p.Ala151=
XM_005254646.1:c.345C>A XP_005254703.1:p.Ala115=
XM_005254647.2:c.345C>A XP_005254704.1:p.Ala115=
XM_005254648.1:c.345C>A XP_005254705.1:p.Ala115=
XM_005254650.2:c.345C>A XP_005254707.1:p.Ala115=
XM_005254651.1:c.345C>A XP_005254708.1:p.Ala115=
XM_005254652.1:c.345C>A XP_005254709.1:p.Ala115=
XM_005254653.1:c.345C>A XP_005254710.1:p.Ala115=
XM_006720667.2:c.453C>A XP_006720730.1:p.Ala151=
XM_006720669.2:c.75C>A XP_006720732.1:p.Ala25=