Canonical Allele Identifier: CA10034324

Gene: TMPRSS2 MX1

Linked Data

• ClinVar Variation Id: 425275
• ClinVar RCV Id: RCV000487647 ; RCV003932791
• dbSNP Id: rs142750000
• ExAC: 21:42839661 C / T
• gnomAD v2: 21-42839661-C-T
• gnomAD v3: 21-41467734-C-T
• gnomAD v4: 21-41467734-C-T
• MyVariant Identifiers: chr21:g.42839661C>T (hg19) ; chr21:g.41467734C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41467734C>T , CM000683.2:g.41467734C>T	GRCh38
NC_000021.8:g.42839661C>T , CM000683.1:g.42839661C>T	GRCh37
NC_000021.7:g.41761531C>T	NCBI36
NG_047085.1:g.45425G>A
NG_047085.2:g.68383G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332149.10:c.1467G>A (TMPRSS2) MANE Select	ENSP00000330330.5:p.Arg489=
ENST00000424093.6:c.1347G>A (TMPRSS2)	ENSP00000397846.2:p.Arg449=
ENST00000454499.6:c.1467G>A (TMPRSS2)	ENSP00000389006.2:p.Arg489=
ENST00000458356.6:c.1467G>A (TMPRSS2)	ENSP00000391216.1:p.Arg489=
ENST00000676973.1:c.1467G>A (TMPRSS2)	ENSP00000504705.1:p.Arg489=
ENST00000677680.1:c.*884G>A (TMPRSS2)	ENSP00000504526.1:n.*884G>A
ENST00000678171.1:c.1467G>A (TMPRSS2)	ENSP00000503877.1:p.Arg489=
ENST00000678348.1:c.1467G>A (TMPRSS2)	ENSP00000503556.1:p.Arg489=
ENST00000678617.1:n.1706G>A (TMPRSS2)
ENST00000678743.1:c.1143G>A (TMPRSS2)	ENSP00000503377.1:p.Arg381=
ENST00000678959.1:c.*1199G>A (TMPRSS2)	ENSP00000503114.1:n.*1199G>A
ENST00000679016.1:c.1260G>A (TMPRSS2)	ENSP00000504610.1:p.Arg420=
ENST00000679054.1:c.1467G>A (TMPRSS2)	ENSP00000502928.1:p.Arg489=
ENST00000679181.1:c.*561G>A (TMPRSS2)	ENSP00000504238.1:n.*561G>A
ENST00000679263.1:c.1626G>A (TMPRSS2)	ENSP00000504602.1:p.Arg542=
ENST00000679386.1:c.1759-503C>T (MX1)	ENSP00000505700.1:n.1759-503C>T
ENST00000332149.9:c.1467G>A (TMPRSS2)	ENSP00000330330.5:p.Arg489=
ENST00000398585.7:c.1578G>A (TMPRSS2)	ENSP00000381588.3:p.Arg526=
ENST00000454499.5:c.1467G>A (TMPRSS2)	ENSP00000389006.1:p.Arg489=
ENST00000458356.5:c.1467G>A (TMPRSS2)	ENSP00000391216.1:p.Arg489=
ENST00000488556.1:n.369G>A (TMPRSS2)
NM_001135099.1:c.1578G>A (TMPRSS2)	NP_001128571.1:p.Arg526=
NM_005656.3:c.1467G>A (TMPRSS2)	NP_005647.3:p.Arg489=
XM_005261043.2:c.1347G>A (TMPRSS2)	XP_005261100.1:p.Arg449=
XM_011529731.1:c.1467G>A (TMPRSS2)	XP_011528033.1:p.Arg489=
XM_011529733.1:c.1143G>A (TMPRSS2)	XP_011528035.1:p.Arg381=
NM_005656.4:c.1467G>A (TMPRSS2) MANE Select	NP_005647.3:p.Arg489=
NM_001382720.1:c.1467G>A (TMPRSS2)	NP_001369649.1:p.Arg489=