Canonical Allele Identifier: CA511459135

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19653456G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281139G>T , CM000683.2:g.18281139G>T	GRCh38
NC_000021.8:g.19653456G>T , CM000683.1:g.19653456G>T	GRCh37
NC_000021.7:g.18575327G>T	NCBI36
NG_012207.1:g.127515C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2569C>A MANE Select	ENSP00000284885.3:p.Arg857=
ENST00000284885.7:c.2569C>A	ENSP00000284885.3:p.Arg857=
NM_002772.2:c.2569C>A	NP_002763.2:p.Arg857=
XM_011529654.1:c.2704C>A	XP_011527956.1:p.Arg902=
XM_011529655.1:c.2704C>A	XP_011527957.1:p.Arg902=
XM_011529656.1:c.2704C>A	XP_011527958.1:p.Arg902=
XM_011529657.1:c.2659C>A	XP_011527959.1:p.Arg887=
XM_011529658.1:c.2623C>A	XP_011527960.1:p.Arg875=
XM_011529659.1:c.2614C>A	XP_011527961.1:p.Arg872=
XM_011529654.2:c.2704C>A	XP_011527956.1:p.Arg902=
XM_011529656.2:c.2704C>A	XP_011527958.1:p.Arg902=
XM_011529657.2:c.2659C>A	XP_011527959.1:p.Arg887=
XM_011529658.2:c.2623C>A	XP_011527960.1:p.Arg875=
NM_002772.3:c.2569C>A MANE Select	NP_002763.3:p.Arg857=