Canonical Allele Identifier: CA409847969

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs2146871328
• MyVariant Identifiers: chr21:g.19653420T>C (hg19) ; chr21:g.18281103T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281103T>C , CM000683.2:g.18281103T>C	GRCh38
NC_000021.8:g.19653420T>C , CM000683.1:g.19653420T>C	GRCh37
NC_000021.7:g.18575291T>C	NCBI36
NG_012207.1:g.127551A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2605A>G MANE Select	ENSP00000284885.3:p.Asn869Asp
ENST00000284885.7:c.2605A>G	ENSP00000284885.3:p.Asn869Asp
NM_002772.2:c.2605A>G	NP_002763.2:p.Asn869Asp
XM_011529654.1:c.2740A>G	XP_011527956.1:p.Asn914Asp
XM_011529655.1:c.2740A>G	XP_011527957.1:p.Asn914Asp
XM_011529656.1:c.2740A>G	XP_011527958.1:p.Asn914Asp
XM_011529657.1:c.2695A>G	XP_011527959.1:p.Asn899Asp
XM_011529658.1:c.2659A>G	XP_011527960.1:p.Asn887Asp
XM_011529659.1:c.2650A>G	XP_011527961.1:p.Asn884Asp
XM_011529654.2:c.2740A>G	XP_011527956.1:p.Asn914Asp
XM_011529656.2:c.2740A>G	XP_011527958.1:p.Asn914Asp
XM_011529657.2:c.2695A>G	XP_011527959.1:p.Asn899Asp
XM_011529658.2:c.2659A>G	XP_011527960.1:p.Asn887Asp
NM_002772.3:c.2605A>G MANE Select	NP_002763.3:p.Asn869Asp