Canonical Allele Identifier: CA410319575

Gene: TMPRSS2

Linked Data

• dbSNP Id: rs1401630535
• gnomAD v2: 21-42852407-A-C
• gnomAD v3: 21-41480480-A-C
• gnomAD v4: 21-41480480-A-C
• MyVariant Identifiers: chr21:g.42852407A>C (hg19) ; chr21:g.41480480A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41480480A>C , CM000683.2:g.41480480A>C	GRCh38
NC_000021.8:g.42852407A>C , CM000683.1:g.42852407A>C	GRCh37
NC_000021.7:g.41774277A>C	NCBI36
NG_047085.1:g.32679T>G
NG_047085.2:g.55637T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332149.10:c.568T>G MANE Select	ENSP00000330330.5:p.Tyr190Asp
ENST00000424093.6:c.448T>G	ENSP00000397846.2:p.Tyr150Asp
ENST00000454499.6:c.568T>G	ENSP00000389006.2:p.Tyr190Asp
ENST00000458356.6:c.568T>G	ENSP00000391216.1:p.Tyr190Asp
ENST00000676973.1:c.568T>G	ENSP00000504705.1:p.Tyr190Asp
ENST00000677680.1:c.568T>G	ENSP00000504526.1:p.Tyr190Asp
ENST00000678171.1:c.568T>G	ENSP00000503877.1:p.Tyr190Asp
ENST00000678348.1:c.568T>G	ENSP00000503556.1:p.Tyr190Asp
ENST00000678617.1:n.807T>G
ENST00000678743.1:c.244T>G	ENSP00000503377.1:p.Tyr82Asp
ENST00000678959.1:c.*300T>G	ENSP00000503114.1:n.*300T>G
ENST00000679016.1:c.361T>G	ENSP00000504610.1:p.Tyr121Asp
ENST00000679054.1:c.568T>G	ENSP00000502928.1:p.Tyr190Asp
ENST00000679181.1:c.568T>G	ENSP00000504238.1:p.Tyr190Asp
ENST00000679263.1:c.727T>G	ENSP00000504602.1:p.Tyr243Asp
ENST00000332149.9:c.568T>G	ENSP00000330330.5:p.Tyr190Asp
ENST00000398585.7:c.679T>G	ENSP00000381588.3:p.Tyr227Asp
ENST00000424093.5:c.448T>G	ENSP00000397846.1:p.Tyr150Asp
ENST00000454499.5:c.568T>G	ENSP00000389006.1:p.Tyr190Asp
ENST00000458356.5:c.568T>G	ENSP00000391216.1:p.Tyr190Asp
NM_001135099.1:c.679T>G	NP_001128571.1:p.Tyr227Asp
NM_005656.3:c.568T>G	NP_005647.3:p.Tyr190Asp
XM_005261043.2:c.448T>G	XP_005261100.1:p.Tyr150Asp
XM_011529731.1:c.568T>G	XP_011528033.1:p.Tyr190Asp
XM_011529732.1:c.568T>G	XP_011528034.1:p.Tyr190Asp
XM_011529733.1:c.244T>G	XP_011528035.1:p.Tyr82Asp
NM_005656.4:c.568T>G MANE Select	NP_005647.3:p.Tyr190Asp
NM_001382720.1:c.568T>G	NP_001369649.1:p.Tyr190Asp