Canonical Allele Identifier: CA2390342273

Gene: TMPRSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41480570C= , CM000683.2:g.41480570C=	GRCh38
NC_000021.8:g.42852497C= , CM000683.1:g.42852497C=	GRCh37
NC_000021.7:g.41774367C=	NCBI36
NG_047085.1:g.32589G=
NG_047085.2:g.55547G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005656.4:c.478G= MANE Select	NP_005647.3:p.Val160=
ENST00000332149.10:c.478G= MANE Select	ENSP00000330330.5:p.Val160=
NM_001135099.1:c.589G=	NP_001128571.1:p.Val197=
NM_001382720.1:c.478G=	NP_001369649.1:p.Val160=
NM_005656.3:c.478G=	NP_005647.3:p.Val160=
ENST00000332149.9:c.478G=	ENSP00000330330.5:p.Val160=
ENST00000398585.7:c.589G=	ENSP00000381588.3:p.Val197=
ENST00000424093.5:c.358G=	ENSP00000397846.1:p.Val120=
ENST00000424093.6:c.358G=	ENSP00000397846.2:p.Val120=
ENST00000454499.5:c.478G=	ENSP00000389006.1:p.Val160=
ENST00000454499.6:c.478G=	ENSP00000389006.2:p.Val160=
ENST00000458356.5:c.478G=	ENSP00000391216.1:p.Val160=
ENST00000458356.6:c.478G=	ENSP00000391216.1:p.Val160=
ENST00000676973.1:c.478G=	ENSP00000504705.1:p.Val160=
ENST00000677680.1:c.478G=	ENSP00000504526.1:p.Val160=
ENST00000678171.1:c.478G=	ENSP00000503877.1:p.Val160=
ENST00000678348.1:c.478G=	ENSP00000503556.1:p.Val160=
ENST00000678617.1:n.717G=
ENST00000678743.1:c.154G=	ENSP00000503377.1:p.Val52=
ENST00000678959.1:c.*210G=	ENSP00000503114.1:n.*210G=
ENST00000679016.1:c.271G=	ENSP00000504610.1:p.Val91=
ENST00000679054.1:c.478G=	ENSP00000502928.1:p.Val160=
ENST00000679181.1:c.478G=	ENSP00000504238.1:p.Val160=
ENST00000679263.1:c.637G=	ENSP00000504602.1:p.Val213=
XM_005261043.2:c.358G=	XP_005261100.1:p.Val120=
XM_011529731.1:c.478G=	XP_011528033.1:p.Val160=
XM_011529732.1:c.478G=	XP_011528034.1:p.Val160=
XM_011529733.1:c.154G=	XP_011528035.1:p.Val52=