Canonical Allele Identifier: CA6281752

Gene: TMPRSS5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113694530C>T , CM000673.2:g.113694530C>T	GRCh38
NC_000011.9:g.113565252C>T , CM000673.1:g.113565252C>T	GRCh37
NC_000011.8:g.113070462C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030770.4:c.733G>A MANE Select	NP_110397.2:p.Gly245Ser
ENST00000299882.11:c.733G>A MANE Select	ENSP00000299882.5:p.Gly245Ser
NM_001288749.1:c.447-1281G>A	NP_001275678.1:n.447-1281G>A
NM_001288749.2:c.447-1281G>A	NP_001275678.1:n.447-1281G>A
NM_001288750.1:c.601G>A	NP_001275679.1:p.Gly201Ser
NM_001288750.2:c.601G>A	NP_001275679.1:p.Gly201Ser
NM_001288751.1:c.706G>A	NP_001275680.1:p.Gly236Ser
NM_001288751.2:c.706G>A	NP_001275680.1:p.Gly236Ser
NM_001288752.1:c.579-1281G>A	NP_001275681.1:n.579-1281G>A
NM_001288752.2:c.579-1281G>A	NP_001275681.1:n.579-1281G>A
NM_030770.3:c.733G>A	NP_110397.2:p.Gly245Ser
NR_110046.1:n.680G>A
NR_110046.2:n.615G>A
NR_110047.1:n.680G>A
NR_110047.2:n.615G>A
ENST00000299882.9:c.733G>A	ENSP00000299882.5:p.Gly245Ser
ENST00000536856.5:c.-45G>A	ENSP00000437937.1:n.-45G>A
ENST00000538770.1:c.-45G>A	ENSP00000445502.1:n.-45G>A
ENST00000538955.5:c.601G>A	ENSP00000445528.1:p.Gly201Ser
ENST00000539732.5:c.-45G>A	ENSP00000443681.1:n.-45G>A
ENST00000540540.5:c.-45G>A	ENSP00000437761.1:n.-45G>A
ENST00000544476.1:c.447-1281G>A	ENSP00000445930.1:n.447-1281G>A
ENST00000544634.5:c.579-1281G>A	ENSP00000440783.1:n.579-1281G>A
ENST00000545579.5:c.706G>A	ENSP00000441104.1:p.Gly236Ser
ENST00000545579.6:c.706G>A	ENSP00000441104.1:p.Gly236Ser
ENST00000645981.1:c.*702G>A	ENSP00000496410.1:n.*702G>A
XM_011543014.1:c.724G>A	XP_011541316.1:p.Gly242Ser
XM_011543015.1:c.733G>A	XP_011541317.1:p.Gly245Ser
XM_011543016.1:c.733G>A	XP_011541318.1:p.Gly245Ser
XM_017018366.1:c.-1186G>A	XP_016873855.1:n.-1186G>A
XM_017018367.1:c.-1186G>A	XP_016873856.1:n.-1186G>A
XR_001747990.1:n.4320G>A
XR_001747991.1:n.4424G>A
XR_001747992.1:n.4217G>A