Canonical Allele Identifier: CA2379744571
Community Standard Title: NM_002772.3(TMPRSS15):c.2194C= (p.Pro732=)
Gene: TMPRSS15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18297801G= , CM000683.2:g.18297801G= GRCh38
NC_000021.8:g.19670118G= , CM000683.1:g.19670118G= GRCh37
NC_000021.7:g.18591989G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002772.3:c.2194C= MANE Select NP_002763.3:p.Pro732=
ENST00000284885.8:c.2194C= MANE Select ENSP00000284885.3:p.Pro732=
ENST00000284885.7:c.2194C= ENSP00000284885.3:p.Pro732=
XM_011529654.1:c.2329C= XP_011527956.1:p.Pro777=
XM_011529654.2:c.2329C= XP_011527956.1:p.Pro777=
XM_011529655.1:c.2329C= XP_011527957.1:p.Pro777=
XM_011529656.1:c.2329C= XP_011527958.1:p.Pro777=
XM_011529656.2:c.2329C= XP_011527958.1:p.Pro777=
XM_011529657.1:c.2284C= XP_011527959.1:p.Pro762=
XM_011529657.2:c.2284C= XP_011527959.1:p.Pro762=
XM_011529658.1:c.2248C= XP_011527960.1:p.Pro750=
XM_011529658.2:c.2248C= XP_011527960.1:p.Pro750=
XM_011529659.1:c.2239C= XP_011527961.1:p.Pro747=