Canonical Allele Identifier: CA228647072
Gene: TMPRSS5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113690763del , CM000673.2:g.113690763del GRCh38
NC_000011.9:g.113561485del , CM000673.1:g.113561485del GRCh37
NC_000011.8:g.113066695del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_030770.4:c.1063+81del MANE Select NP_110397.2:n.1063+81del
ENST00000299882.11:c.1063+81del MANE Select ENSP00000299882.5:n.1063+81del
NM_001288749.1:c.724+81del NP_001275678.1:n.724+81del
NM_001288749.2:c.724+81del NP_001275678.1:n.724+81del
NM_001288750.1:c.931+81del NP_001275679.1:n.931+81del
NM_001288750.2:c.931+81del NP_001275679.1:n.931+81del
NM_001288751.1:c.1036+81del NP_001275680.1:n.1036+81del
NM_001288751.2:c.1036+81del NP_001275680.1:n.1036+81del
NM_001288752.1:c.856+81del NP_001275681.1:n.856+81del
NM_001288752.2:c.856+81del NP_001275681.1:n.856+81del
NM_030770.3:c.1063+81del NP_110397.2:n.1063+81del
NR_110046.1:n.1010+81del
NR_110046.2:n.945+81del
NR_110047.1:n.1010+81del
NR_110047.2:n.945+81del
ENST00000299882.9:c.1063+81del ENSP00000299882.5:n.1063+81del
ENST00000536856.5:c.286+81del ENSP00000437937.1:n.286+81del
ENST00000538955.5:c.931+81del ENSP00000445528.1:n.931+81del
ENST00000540540.5:c.286+81del ENSP00000437761.1:n.286+81del
ENST00000544476.1:c.724+81del ENSP00000445930.1:n.724+81del
ENST00000544634.5:c.856+81del ENSP00000440783.1:n.856+81del
ENST00000545265.5:n.412+81del
ENST00000545579.5:c.1036+81del ENSP00000441104.1:n.1036+81del
ENST00000545579.6:c.1036+81del ENSP00000441104.1:n.1036+81del
ENST00000645981.1:c.*1032+81del ENSP00000496410.1:n.*1032+81del
XM_011543014.1:c.1054+81del XP_011541316.1:n.1054+81del
XM_011543015.1:c.1063+81del XP_011541317.1:n.1063+81del
XM_017018366.1:c.373+81del XP_016873855.1:n.373+81del
XM_017018367.1:c.373+81del XP_016873856.1:n.373+81del
XR_001747990.1:n.5878+81del
XR_001747991.1:n.5982+81del
XR_001747992.1:n.5775+81del