Canonical Allele Identifier: CA409847904

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653392G>T (hg19) ; chr21:g.18281075G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281075G>T , CM000683.2:g.18281075G>T	GRCh38
NC_000021.8:g.19653392G>T , CM000683.1:g.19653392G>T	GRCh37
NC_000021.7:g.18575263G>T	NCBI36
NG_012207.1:g.127579C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2633C>A MANE Select	ENSP00000284885.3:p.Ala878Asp
ENST00000284885.7:c.2633C>A	ENSP00000284885.3:p.Ala878Asp
NM_002772.2:c.2633C>A	NP_002763.2:p.Ala878Asp
XM_011529654.1:c.2768C>A	XP_011527956.1:p.Ala923Asp
XM_011529655.1:c.2768C>A	XP_011527957.1:p.Ala923Asp
XM_011529656.1:c.2768C>A	XP_011527958.1:p.Ala923Asp
XM_011529657.1:c.2723C>A	XP_011527959.1:p.Ala908Asp
XM_011529658.1:c.2687C>A	XP_011527960.1:p.Ala896Asp
XM_011529659.1:c.2678C>A	XP_011527961.1:p.Ala893Asp
XM_011529654.2:c.2768C>A	XP_011527956.1:p.Ala923Asp
XM_011529656.2:c.2768C>A	XP_011527958.1:p.Ala923Asp
XM_011529657.2:c.2723C>A	XP_011527959.1:p.Ala908Asp
XM_011529658.2:c.2687C>A	XP_011527960.1:p.Ala896Asp
NM_002772.3:c.2633C>A MANE Select	NP_002763.3:p.Ala878Asp