Canonical Allele Identifier: CA511459167
Gene: TMPRSS15 HGNC NCBI

Linked Data

dbSNP Id: rs1428717560

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281181G>A , CM000683.2:g.18281181G>A GRCh38
NC_000021.8:g.19653498G>A , CM000683.1:g.19653498G>A GRCh37
NC_000021.7:g.18575369G>A NCBI36
NG_012207.1:g.127473C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000284885.8:c.2527C>T MANE Select ENSP00000284885.3:p.Leu843=
ENST00000284885.7:c.2527C>T ENSP00000284885.3:p.Leu843=
NM_002772.2:c.2527C>T NP_002763.2:p.Leu843=
XM_011529654.1:c.2662C>T XP_011527956.1:p.Leu888=
XM_011529655.1:c.2662C>T XP_011527957.1:p.Leu888=
XM_011529656.1:c.2662C>T XP_011527958.1:p.Leu888=
XM_011529657.1:c.2617C>T XP_011527959.1:p.Leu873=
XM_011529658.1:c.2581C>T XP_011527960.1:p.Leu861=
XM_011529659.1:c.2572C>T XP_011527961.1:p.Leu858=
XM_011529654.2:c.2662C>T XP_011527956.1:p.Leu888=
XM_011529656.2:c.2662C>T XP_011527958.1:p.Leu888=
XM_011529657.2:c.2617C>T XP_011527959.1:p.Leu873=
XM_011529658.2:c.2581C>T XP_011527960.1:p.Leu861=
NM_002772.3:c.2527C>T MANE Select NP_002763.3:p.Leu843=