Canonical Allele Identifier: CA6281770
Gene: TMPRSS5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113694631G>A , CM000673.2:g.113694631G>A GRCh38
NC_000011.9:g.113565353G>A , CM000673.1:g.113565353G>A GRCh37
NC_000011.8:g.113070563G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_030770.4:c.632C>T MANE Select NP_110397.2:p.Ala211Val
ENST00000299882.11:c.632C>T MANE Select ENSP00000299882.5:p.Ala211Val
NM_001288749.1:c.447-1382C>T NP_001275678.1:n.447-1382C>T
NM_001288749.2:c.447-1382C>T NP_001275678.1:n.447-1382C>T
NM_001288750.1:c.500C>T NP_001275679.1:p.Ala167Val
NM_001288750.2:c.500C>T NP_001275679.1:p.Ala167Val
NM_001288751.1:c.605C>T NP_001275680.1:p.Ala202Val
NM_001288751.2:c.605C>T NP_001275680.1:p.Ala202Val
NM_001288752.1:c.579-1382C>T NP_001275681.1:n.579-1382C>T
NM_001288752.2:c.579-1382C>T NP_001275681.1:n.579-1382C>T
NM_030770.3:c.632C>T NP_110397.2:p.Ala211Val
NR_110046.1:n.579C>T
NR_110046.2:n.514C>T
NR_110047.1:n.579C>T
NR_110047.2:n.514C>T
ENST00000299882.9:c.632C>T ENSP00000299882.5:p.Ala211Val
ENST00000536856.5:c.-146C>T ENSP00000437937.1:n.-146C>T
ENST00000538770.1:c.-146C>T ENSP00000445502.1:n.-146C>T
ENST00000538955.5:c.500C>T ENSP00000445528.1:p.Ala167Val
ENST00000539732.5:c.-146C>T ENSP00000443681.1:n.-146C>T
ENST00000540540.5:c.-146C>T ENSP00000437761.1:n.-146C>T
ENST00000544476.1:c.447-1382C>T ENSP00000445930.1:n.447-1382C>T
ENST00000544634.5:c.579-1382C>T ENSP00000440783.1:n.579-1382C>T
ENST00000545579.5:c.605C>T ENSP00000441104.1:p.Ala202Val
ENST00000545579.6:c.605C>T ENSP00000441104.1:p.Ala202Val
ENST00000645981.1:c.*601C>T ENSP00000496410.1:n.*601C>T
XM_011543014.1:c.623C>T XP_011541316.1:p.Ala208Val
XM_011543015.1:c.632C>T XP_011541317.1:p.Ala211Val
XM_011543016.1:c.632C>T XP_011541318.1:p.Ala211Val
XM_017018366.1:c.-1287C>T XP_016873855.1:n.-1287C>T
XM_017018367.1:c.-1287C>T XP_016873856.1:n.-1287C>T
XR_001747990.1:n.4219C>T
XR_001747991.1:n.4323C>T
XR_001747992.1:n.4116C>T