Canonical Allele Identifier: CA2379736691
Gene: TMPRSS15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281148T= , CM000683.2:g.18281148T= GRCh38
NC_000021.8:g.19653465T= , CM000683.1:g.19653465T= GRCh37
NC_000021.7:g.18575336T= NCBI36
NG_012207.1:g.127506A=

Transcript Alleles

HGVS Amino-acid change
ENST00000284885.8:c.2560A= MANE Select ENSP00000284885.3:p.Thr854=
ENST00000284885.7:c.2560A= ENSP00000284885.3:p.Thr854=
NM_002772.2:c.2560A= NP_002763.2:p.Thr854=
XM_011529654.1:c.2695A= XP_011527956.1:p.Thr899=
XM_011529655.1:c.2695A= XP_011527957.1:p.Thr899=
XM_011529656.1:c.2695A= XP_011527958.1:p.Thr899=
XM_011529657.1:c.2650A= XP_011527959.1:p.Thr884=
XM_011529658.1:c.2614A= XP_011527960.1:p.Thr872=
XM_011529659.1:c.2605A= XP_011527961.1:p.Thr869=
XM_011529654.2:c.2695A= XP_011527956.1:p.Thr899=
XM_011529656.2:c.2695A= XP_011527958.1:p.Thr899=
XM_011529657.2:c.2650A= XP_011527959.1:p.Thr884=
XM_011529658.2:c.2614A= XP_011527960.1:p.Thr872=
NM_002772.3:c.2560A= MANE Select NP_002763.3:p.Thr854=