Canonical Allele Identifier: CA2379736654
Gene: TMPRSS15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281083G= , CM000683.2:g.18281083G= GRCh38
NC_000021.8:g.19653400G= , CM000683.1:g.19653400G= GRCh37
NC_000021.7:g.18575271G= NCBI36
NG_012207.1:g.127571C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284885.8:c.2625C= MANE Select ENSP00000284885.3:p.Asn875=
ENST00000284885.7:c.2625C= ENSP00000284885.3:p.Asn875=
NM_002772.2:c.2625C= NP_002763.2:p.Asn875=
XM_011529654.1:c.2760C= XP_011527956.1:p.Asn920=
XM_011529655.1:c.2760C= XP_011527957.1:p.Asn920=
XM_011529656.1:c.2760C= XP_011527958.1:p.Asn920=
XM_011529657.1:c.2715C= XP_011527959.1:p.Asn905=
XM_011529658.1:c.2679C= XP_011527960.1:p.Asn893=
XM_011529659.1:c.2670C= XP_011527961.1:p.Asn890=
XM_011529654.2:c.2760C= XP_011527956.1:p.Asn920=
XM_011529656.2:c.2760C= XP_011527958.1:p.Asn920=
XM_011529657.2:c.2715C= XP_011527959.1:p.Asn905=
XM_011529658.2:c.2679C= XP_011527960.1:p.Asn893=
NM_002772.3:c.2625C= MANE Select NP_002763.3:p.Asn875=