Canonical Allele Identifier: CA410319981

Gene: TMPRSS2

Linked Data

• MyVariant Identifiers: chr21:g.42852499T>A (hg19) ; chr21:g.41480572T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41480572T>A , CM000683.2:g.41480572T>A	GRCh38
NC_000021.8:g.42852499T>A , CM000683.1:g.42852499T>A	GRCh37
NC_000021.7:g.41774369T>A	NCBI36
NG_047085.1:g.32587A>T
NG_047085.2:g.55545A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000332149.10:c.476A>T MANE Select	ENSP00000330330.5:p.Gln159Leu
ENST00000424093.6:c.356A>T	ENSP00000397846.2:p.Gln119Leu
ENST00000454499.6:c.476A>T	ENSP00000389006.2:p.Gln159Leu
ENST00000458356.6:c.476A>T	ENSP00000391216.1:p.Gln159Leu
ENST00000676973.1:c.476A>T	ENSP00000504705.1:p.Gln159Leu
ENST00000677680.1:c.476A>T	ENSP00000504526.1:p.Gln159Leu
ENST00000678171.1:c.476A>T	ENSP00000503877.1:p.Gln159Leu
ENST00000678348.1:c.476A>T	ENSP00000503556.1:p.Gln159Leu
ENST00000678617.1:n.715A>T
ENST00000678743.1:c.152A>T	ENSP00000503377.1:p.Gln51Leu
ENST00000678959.1:c.*208A>T	ENSP00000503114.1:n.*208A>T
ENST00000679016.1:c.269A>T	ENSP00000504610.1:p.Gln90Leu
ENST00000679054.1:c.476A>T	ENSP00000502928.1:p.Gln159Leu
ENST00000679181.1:c.476A>T	ENSP00000504238.1:p.Gln159Leu
ENST00000679263.1:c.635A>T	ENSP00000504602.1:p.Gln212Leu
ENST00000332149.9:c.476A>T	ENSP00000330330.5:p.Gln159Leu
ENST00000398585.7:c.587A>T	ENSP00000381588.3:p.Gln196Leu
ENST00000424093.5:c.356A>T	ENSP00000397846.1:p.Gln119Leu
ENST00000454499.5:c.476A>T	ENSP00000389006.1:p.Gln159Leu
ENST00000458356.5:c.476A>T	ENSP00000391216.1:p.Gln159Leu
NM_001135099.1:c.587A>T	NP_001128571.1:p.Gln196Leu
NM_005656.3:c.476A>T	NP_005647.3:p.Gln159Leu
XM_005261043.2:c.356A>T	XP_005261100.1:p.Gln119Leu
XM_011529731.1:c.476A>T	XP_011528033.1:p.Gln159Leu
XM_011529732.1:c.476A>T	XP_011528034.1:p.Gln159Leu
XM_011529733.1:c.152A>T	XP_011528035.1:p.Gln51Leu
NM_005656.4:c.476A>T MANE Select	NP_005647.3:p.Gln159Leu
NM_001382720.1:c.476A>T	NP_001369649.1:p.Gln159Leu