Canonical Allele Identifier: CA409847867
Gene: TMPRSS15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281059T>A , CM000683.2:g.18281059T>A GRCh38
NC_000021.8:g.19653376T>A , CM000683.1:g.19653376T>A GRCh37
NC_000021.7:g.18575247T>A NCBI36
NG_012207.1:g.127595A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284885.8:c.2649A>T MANE Select ENSP00000284885.3:p.Glu883Asp
ENST00000284885.7:c.2649A>T ENSP00000284885.3:p.Glu883Asp
NM_002772.2:c.2649A>T NP_002763.2:p.Glu883Asp
XM_011529654.1:c.2784A>T XP_011527956.1:p.Glu928Asp
XM_011529655.1:c.2784A>T XP_011527957.1:p.Glu928Asp
XM_011529656.1:c.2784A>T XP_011527958.1:p.Glu928Asp
XM_011529657.1:c.2739A>T XP_011527959.1:p.Glu913Asp
XM_011529658.1:c.2703A>T XP_011527960.1:p.Glu901Asp
XM_011529659.1:c.2694A>T XP_011527961.1:p.Glu898Asp
XM_011529654.2:c.2784A>T XP_011527956.1:p.Glu928Asp
XM_011529656.2:c.2784A>T XP_011527958.1:p.Glu928Asp
XM_011529657.2:c.2739A>T XP_011527959.1:p.Glu913Asp
XM_011529658.2:c.2703A>T XP_011527960.1:p.Glu901Asp
NM_002772.3:c.2649A>T MANE Select NP_002763.3:p.Glu883Asp