Canonical Allele Identifier: CA9983982
Gene: TMPRSS15 HGNC NCBI

Linked Data

dbSNP Id: rs753997878

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18281042_18281045del , CM000683.2:g.18281042_18281045del GRCh38
NC_000021.8:g.19653359_19653362del , CM000683.1:g.19653359_19653362del GRCh37
NC_000021.7:g.18575230_18575233del NCBI36
NG_012207.1:g.127610_127613del

Transcript Alleles

HGVS Amino-acid change
ENST00000284885.8:c.2664_2667del MANE Select ENSP00000284885.3:p.Tyr888Ter
ENST00000284885.7:c.2664_2667del ENSP00000284885.3:p.Tyr888Ter
NM_002772.2:c.2664_2667del NP_002763.2:p.Tyr888Ter
XM_011529654.1:c.2799_2802del XP_011527956.1:p.Tyr933Ter
XM_011529655.1:c.2799_2802del XP_011527957.1:p.Tyr933Ter
XM_011529656.1:c.2799_2802del XP_011527958.1:p.Tyr933Ter
XM_011529657.1:c.2754_2757del XP_011527959.1:p.Tyr918Ter
XM_011529658.1:c.2718_2721del XP_011527960.1:p.Tyr906Ter
XM_011529659.1:c.2709_2712del XP_011527961.1:p.Tyr903Ter
XM_011529654.2:c.2799_2802del XP_011527956.1:p.Tyr933Ter
XM_011529656.2:c.2799_2802del XP_011527958.1:p.Tyr933Ter
XM_011529657.2:c.2754_2757del XP_011527959.1:p.Tyr918Ter
XM_011529658.2:c.2718_2721del XP_011527960.1:p.Tyr906Ter
NM_002772.3:c.2664_2667del MANE Select NP_002763.3:p.Tyr888Ter