Canonical Allele Identifier: CA2379736633
Gene: TMPRSS15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281040C= , CM000683.2:g.18281040C= GRCh38
NC_000021.8:g.19653357C= , CM000683.1:g.19653357C= GRCh37
NC_000021.7:g.18575228C= NCBI36
NG_012207.1:g.127614G=

Transcript Alleles

HGVS Amino-acid change
ENST00000284885.8:c.2668G= MANE Select ENSP00000284885.3:p.Asp890=
ENST00000284885.7:c.2668G= ENSP00000284885.3:p.Asp890=
NM_002772.2:c.2668G= NP_002763.2:p.Asp890=
XM_011529654.1:c.2803G= XP_011527956.1:p.Asp935=
XM_011529655.1:c.2803G= XP_011527957.1:p.Asp935=
XM_011529656.1:c.2803G= XP_011527958.1:p.Asp935=
XM_011529657.1:c.2758G= XP_011527959.1:p.Asp920=
XM_011529658.1:c.2722G= XP_011527960.1:p.Asp908=
XM_011529659.1:c.2713G= XP_011527961.1:p.Asp905=
XM_011529654.2:c.2803G= XP_011527956.1:p.Asp935=
XM_011529656.2:c.2803G= XP_011527958.1:p.Asp935=
XM_011529657.2:c.2758G= XP_011527959.1:p.Asp920=
XM_011529658.2:c.2722G= XP_011527960.1:p.Asp908=
NM_002772.3:c.2668G= MANE Select NP_002763.3:p.Asp890=