Canonical Allele Identifier: CA511460494

Gene: TMPRSS15

Linked Data

• MyVariant Identifiers: chr21:g.19685294A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18312977A>T , CM000683.2:g.18312977A>T	GRCh38
NC_000021.8:g.19685294A>T , CM000683.1:g.19685294A>T	GRCh37
NC_000021.7:g.18607165A>T	NCBI36
NG_012207.1:g.95677T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000284885.8:c.2133T>A MANE Select	ENSP00000284885.3:p.Ile711=
ENST00000284885.7:c.2133T>A	ENSP00000284885.3:p.Ile711=
NM_002772.2:c.2133T>A	NP_002763.2:p.Ile711=
XM_011529654.1:c.2268T>A	XP_011527956.1:p.Ile756=
XM_011529655.1:c.2268T>A	XP_011527957.1:p.Ile756=
XM_011529656.1:c.2268T>A	XP_011527958.1:p.Ile756=
XM_011529657.1:c.2223T>A	XP_011527959.1:p.Ile741=
XM_011529658.1:c.2187T>A	XP_011527960.1:p.Ile729=
XM_011529659.1:c.2178T>A	XP_011527961.1:p.Ile726=
XM_011529654.2:c.2268T>A	XP_011527956.1:p.Ile756=
XM_011529656.2:c.2268T>A	XP_011527958.1:p.Ile756=
XM_011529657.2:c.2223T>A	XP_011527959.1:p.Ile741=
XM_011529658.2:c.2187T>A	XP_011527960.1:p.Ile729=
NM_002772.3:c.2133T>A MANE Select	NP_002763.3:p.Ile711=