Canonical Allele Identifier: CA410320024

Gene: TMPRSS2

Linked Data

• dbSNP Id: rs2146452172
• gnomAD v4: 21-41480581-A-G
• MyVariant Identifiers: chr21:g.42852508A>G (hg19) ; chr21:g.41480581A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41480581A>G , CM000683.2:g.41480581A>G	GRCh38
NC_000021.8:g.42852508A>G , CM000683.1:g.42852508A>G	GRCh37
NC_000021.7:g.41774378A>G	NCBI36
NG_047085.1:g.32578T>C
NG_047085.2:g.55536T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332149.10:c.467T>C MANE Select	ENSP00000330330.5:p.Phe156Ser
ENST00000424093.6:c.347T>C	ENSP00000397846.2:p.Phe116Ser
ENST00000454499.6:c.467T>C	ENSP00000389006.2:p.Phe156Ser
ENST00000458356.6:c.467T>C	ENSP00000391216.1:p.Phe156Ser
ENST00000676973.1:c.467T>C	ENSP00000504705.1:p.Phe156Ser
ENST00000677680.1:c.467T>C	ENSP00000504526.1:p.Phe156Ser
ENST00000678171.1:c.467T>C	ENSP00000503877.1:p.Phe156Ser
ENST00000678348.1:c.467T>C	ENSP00000503556.1:p.Phe156Ser
ENST00000678617.1:n.706T>C
ENST00000678743.1:c.143T>C	ENSP00000503377.1:p.Phe48Ser
ENST00000678959.1:c.*199T>C	ENSP00000503114.1:n.*199T>C
ENST00000679016.1:c.260T>C	ENSP00000504610.1:p.Phe87Ser
ENST00000679054.1:c.467T>C	ENSP00000502928.1:p.Phe156Ser
ENST00000679181.1:c.467T>C	ENSP00000504238.1:p.Phe156Ser
ENST00000679263.1:c.626T>C	ENSP00000504602.1:p.Phe209Ser
ENST00000332149.9:c.467T>C	ENSP00000330330.5:p.Phe156Ser
ENST00000398585.7:c.578T>C	ENSP00000381588.3:p.Phe193Ser
ENST00000424093.5:c.347T>C	ENSP00000397846.1:p.Phe116Ser
ENST00000454499.5:c.467T>C	ENSP00000389006.1:p.Phe156Ser
ENST00000458356.5:c.467T>C	ENSP00000391216.1:p.Phe156Ser
NM_001135099.1:c.578T>C	NP_001128571.1:p.Phe193Ser
NM_005656.3:c.467T>C	NP_005647.3:p.Phe156Ser
XM_005261043.2:c.347T>C	XP_005261100.1:p.Phe116Ser
XM_011529731.1:c.467T>C	XP_011528033.1:p.Phe156Ser
XM_011529732.1:c.467T>C	XP_011528034.1:p.Phe156Ser
XM_011529733.1:c.143T>C	XP_011528035.1:p.Phe48Ser
NM_005656.4:c.467T>C MANE Select	NP_005647.3:p.Phe156Ser
NM_001382720.1:c.467T>C	NP_001369649.1:p.Phe156Ser