Canonical Allele Identifier: CA410319991

Gene: TMPRSS2

Linked Data

• MyVariant Identifiers: chr21:g.42852502A>G (hg19) ; chr21:g.41480575A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41480575A>G , CM000683.2:g.41480575A>G	GRCh38
NC_000021.8:g.42852502A>G , CM000683.1:g.42852502A>G	GRCh37
NC_000021.7:g.41774372A>G	NCBI36
NG_047085.1:g.32584T>C
NG_047085.2:g.55542T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000332149.10:c.473T>C MANE Select	ENSP00000330330.5:p.Leu158Pro
ENST00000424093.6:c.353T>C	ENSP00000397846.2:p.Leu118Pro
ENST00000454499.6:c.473T>C	ENSP00000389006.2:p.Leu158Pro
ENST00000458356.6:c.473T>C	ENSP00000391216.1:p.Leu158Pro
ENST00000676973.1:c.473T>C	ENSP00000504705.1:p.Leu158Pro
ENST00000677680.1:c.473T>C	ENSP00000504526.1:p.Leu158Pro
ENST00000678171.1:c.473T>C	ENSP00000503877.1:p.Leu158Pro
ENST00000678348.1:c.473T>C	ENSP00000503556.1:p.Leu158Pro
ENST00000678617.1:n.712T>C
ENST00000678743.1:c.149T>C	ENSP00000503377.1:p.Leu50Pro
ENST00000678959.1:c.*205T>C	ENSP00000503114.1:n.*205T>C
ENST00000679016.1:c.266T>C	ENSP00000504610.1:p.Leu89Pro
ENST00000679054.1:c.473T>C	ENSP00000502928.1:p.Leu158Pro
ENST00000679181.1:c.473T>C	ENSP00000504238.1:p.Leu158Pro
ENST00000679263.1:c.632T>C	ENSP00000504602.1:p.Leu211Pro
ENST00000332149.9:c.473T>C	ENSP00000330330.5:p.Leu158Pro
ENST00000398585.7:c.584T>C	ENSP00000381588.3:p.Leu195Pro
ENST00000424093.5:c.353T>C	ENSP00000397846.1:p.Leu118Pro
ENST00000454499.5:c.473T>C	ENSP00000389006.1:p.Leu158Pro
ENST00000458356.5:c.473T>C	ENSP00000391216.1:p.Leu158Pro
NM_001135099.1:c.584T>C	NP_001128571.1:p.Leu195Pro
NM_005656.3:c.473T>C	NP_005647.3:p.Leu158Pro
XM_005261043.2:c.353T>C	XP_005261100.1:p.Leu118Pro
XM_011529731.1:c.473T>C	XP_011528033.1:p.Leu158Pro
XM_011529732.1:c.473T>C	XP_011528034.1:p.Leu158Pro
XM_011529733.1:c.149T>C	XP_011528035.1:p.Leu50Pro
NM_005656.4:c.473T>C MANE Select	NP_005647.3:p.Leu158Pro
NM_001382720.1:c.473T>C	NP_001369649.1:p.Leu158Pro