Canonical Allele Identifier: CA13574390

Gene: TMPRSS5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113692966A>G , CM000673.2:g.113692966A>G	GRCh38
NC_000011.9:g.113563688A>G , CM000673.1:g.113563688A>G	GRCh37
NC_000011.8:g.113068898A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030770.4:c.964+105T>C MANE Select	NP_110397.2:n.964+105T>C
ENST00000299882.11:c.964+105T>C MANE Select	ENSP00000299882.5:n.964+105T>C
NM_001288749.1:c.625+105T>C	NP_001275678.1:n.625+105T>C
NM_001288749.2:c.625+105T>C	NP_001275678.1:n.625+105T>C
NM_001288750.1:c.832+105T>C	NP_001275679.1:n.832+105T>C
NM_001288750.2:c.832+105T>C	NP_001275679.1:n.832+105T>C
NM_001288751.1:c.937+105T>C	NP_001275680.1:n.937+105T>C
NM_001288751.2:c.937+105T>C	NP_001275680.1:n.937+105T>C
NM_001288752.1:c.757+105T>C	NP_001275681.1:n.757+105T>C
NM_001288752.2:c.757+105T>C	NP_001275681.1:n.757+105T>C
NM_030770.3:c.964+105T>C	NP_110397.2:n.964+105T>C
NR_110046.1:n.911+105T>C
NR_110046.2:n.846+105T>C
NR_110047.1:n.911+105T>C
NR_110047.2:n.846+105T>C
ENST00000299882.9:c.964+105T>C	ENSP00000299882.5:n.964+105T>C
ENST00000536856.5:c.187+105T>C	ENSP00000437937.1:n.187+105T>C
ENST00000538955.5:c.832+105T>C	ENSP00000445528.1:n.832+105T>C
ENST00000540540.5:c.187+105T>C	ENSP00000437761.1:n.187+105T>C
ENST00000544476.1:c.625+105T>C	ENSP00000445930.1:n.625+105T>C
ENST00000544634.5:c.757+105T>C	ENSP00000440783.1:n.757+105T>C
ENST00000545265.5:n.313+105T>C
ENST00000545412.1:n.233+105T>C
ENST00000545579.5:c.937+105T>C	ENSP00000441104.1:n.937+105T>C
ENST00000545579.6:c.937+105T>C	ENSP00000441104.1:n.937+105T>C
ENST00000645981.1:c.*933+105T>C	ENSP00000496410.1:n.*933+105T>C
XM_011543014.1:c.955+105T>C	XP_011541316.1:n.955+105T>C
XM_011543015.1:c.964+105T>C	XP_011541317.1:n.964+105T>C
XM_011543016.1:c.*27+105T>C	XP_011541318.1:n.*27+105T>C
XM_017018366.1:c.274+105T>C	XP_016873855.1:n.274+105T>C
XM_017018367.1:c.274+105T>C	XP_016873856.1:n.274+105T>C
XR_001747990.1:n.5779+105T>C
XR_001747991.1:n.5883+105T>C
XR_001747992.1:n.5676+105T>C