Canonical Allele Identifier: CA6281595
Gene: TMPRSS5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113690247C>T , CM000673.2:g.113690247C>T GRCh38
NC_000011.9:g.113560969C>T , CM000673.1:g.113560969C>T GRCh37
NC_000011.8:g.113066179C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000299882.11:c.1190G>A MANE Select ENSP00000299882.5:p.Arg397Lys
ENST00000545579.6:c.1163G>A ENSP00000441104.1:p.Arg388Lys
ENST00000645981.1:c.*1159G>A ENSP00000496410.1:n.*1159G>A
ENST00000299882.9:c.1190G>A ENSP00000299882.5:p.Arg397Lys
ENST00000536856.5:c.413G>A ENSP00000437937.1:p.Arg138Lys
ENST00000538955.5:c.1058G>A ENSP00000445528.1:p.Arg353Lys
ENST00000540540.5:c.413G>A ENSP00000437761.1:p.Arg138Lys
ENST00000544476.1:c.851G>A ENSP00000445930.1:p.Arg284Lys
ENST00000544634.5:c.983G>A ENSP00000440783.1:p.Arg328Lys
ENST00000545265.5:n.539G>A
ENST00000545579.5:c.1163G>A ENSP00000441104.1:p.Arg388Lys
NM_001288749.1:c.851G>A NP_001275678.1:p.Arg284Lys
NM_001288750.1:c.1058G>A NP_001275679.1:p.Arg353Lys
NM_001288751.1:c.1163G>A NP_001275680.1:p.Arg388Lys
NM_001288752.1:c.983G>A NP_001275681.1:p.Arg328Lys
NM_030770.3:c.1190G>A NP_110397.2:p.Arg397Lys
NR_110046.1:n.1137G>A
NR_110047.1:n.1137G>A
XM_011543014.1:c.1181G>A XP_011541316.1:p.Arg394Lys
XM_011543015.1:c.1190G>A XP_011541317.1:p.Arg397Lys
XM_017018366.1:c.500G>A XP_016873855.1:p.Arg167Lys
XM_017018367.1:c.500G>A XP_016873856.1:p.Arg167Lys
XR_001747990.1:n.6005G>A
XR_001747991.1:n.6109G>A
XR_001747992.1:n.5902G>A
NM_030770.4:c.1190G>A MANE Select NP_110397.2:p.Arg397Lys
NM_001288749.2:c.851G>A NP_001275678.1:p.Arg284Lys
NM_001288750.2:c.1058G>A NP_001275679.1:p.Arg353Lys
NM_001288752.2:c.983G>A NP_001275681.1:p.Arg328Lys
NR_110046.2:n.1072G>A
NR_110047.2:n.1072G>A
NM_001288751.2:c.1163G>A NP_001275680.1:p.Arg388Lys