Canonical Allele Identifier: CA409848153

Gene: TMPRSS15

Linked Data

• dbSNP Id: rs1568979898
• gnomAD v4: 21-18281192-G-T
• MyVariant Identifiers: chr21:g.19653509G>T (hg19) ; chr21:g.18281192G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281192G>T , CM000683.2:g.18281192G>T	GRCh38
NC_000021.8:g.19653509G>T , CM000683.1:g.19653509G>T	GRCh37
NC_000021.7:g.18575380G>T	NCBI36
NG_012207.1:g.127462C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2516C>A MANE Select	ENSP00000284885.3:p.Ala839Glu
ENST00000284885.7:c.2516C>A	ENSP00000284885.3:p.Ala839Glu
NM_002772.2:c.2516C>A	NP_002763.2:p.Ala839Glu
XM_011529654.1:c.2651C>A	XP_011527956.1:p.Ala884Glu
XM_011529655.1:c.2651C>A	XP_011527957.1:p.Ala884Glu
XM_011529656.1:c.2651C>A	XP_011527958.1:p.Ala884Glu
XM_011529657.1:c.2606C>A	XP_011527959.1:p.Ala869Glu
XM_011529658.1:c.2570C>A	XP_011527960.1:p.Ala857Glu
XM_011529659.1:c.2561C>A	XP_011527961.1:p.Ala854Glu
XM_011529654.2:c.2651C>A	XP_011527956.1:p.Ala884Glu
XM_011529656.2:c.2651C>A	XP_011527958.1:p.Ala884Glu
XM_011529657.2:c.2606C>A	XP_011527959.1:p.Ala869Glu
XM_011529658.2:c.2570C>A	XP_011527960.1:p.Ala857Glu
NM_002772.3:c.2516C>A MANE Select	NP_002763.3:p.Ala839Glu