Canonical Allele Identifier: CA410319589

Gene: TMPRSS2

Linked Data

• dbSNP Id: rs1169823484
• MyVariant Identifiers: chr21:g.42852411C>A (hg19) ; chr21:g.41480484C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41480484C>A , CM000683.2:g.41480484C>A	GRCh38
NC_000021.8:g.42852411C>A , CM000683.1:g.42852411C>A	GRCh37
NC_000021.7:g.41774281C>A	NCBI36
NG_047085.1:g.32675G>T
NG_047085.2:g.55633G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332149.10:c.564G>T MANE Select	ENSP00000330330.5:p.Met188Ile
ENST00000424093.6:c.444G>T	ENSP00000397846.2:p.Met148Ile
ENST00000454499.6:c.564G>T	ENSP00000389006.2:p.Met188Ile
ENST00000458356.6:c.564G>T	ENSP00000391216.1:p.Met188Ile
ENST00000676973.1:c.564G>T	ENSP00000504705.1:p.Met188Ile
ENST00000677680.1:c.564G>T	ENSP00000504526.1:p.Met188Ile
ENST00000678171.1:c.564G>T	ENSP00000503877.1:p.Met188Ile
ENST00000678348.1:c.564G>T	ENSP00000503556.1:p.Met188Ile
ENST00000678617.1:n.803G>T
ENST00000678743.1:c.240G>T	ENSP00000503377.1:p.Met80Ile
ENST00000678959.1:c.*296G>T	ENSP00000503114.1:n.*296G>T
ENST00000679016.1:c.357G>T	ENSP00000504610.1:p.Met119Ile
ENST00000679054.1:c.564G>T	ENSP00000502928.1:p.Met188Ile
ENST00000679181.1:c.564G>T	ENSP00000504238.1:p.Met188Ile
ENST00000679263.1:c.723G>T	ENSP00000504602.1:p.Met241Ile
ENST00000332149.9:c.564G>T	ENSP00000330330.5:p.Met188Ile
ENST00000398585.7:c.675G>T	ENSP00000381588.3:p.Met225Ile
ENST00000424093.5:c.444G>T	ENSP00000397846.1:p.Met148Ile
ENST00000454499.5:c.564G>T	ENSP00000389006.1:p.Met188Ile
ENST00000458356.5:c.564G>T	ENSP00000391216.1:p.Met188Ile
NM_001135099.1:c.675G>T	NP_001128571.1:p.Met225Ile
NM_005656.3:c.564G>T	NP_005647.3:p.Met188Ile
XM_005261043.2:c.444G>T	XP_005261100.1:p.Met148Ile
XM_011529731.1:c.564G>T	XP_011528033.1:p.Met188Ile
XM_011529732.1:c.564G>T	XP_011528034.1:p.Met188Ile
XM_011529733.1:c.240G>T	XP_011528035.1:p.Met80Ile
NM_005656.4:c.564G>T MANE Select	NP_005647.3:p.Met188Ile
NM_001382720.1:c.564G>T	NP_001369649.1:p.Met188Ile