Canonical Allele Identifier: CA1020838280
Gene: TMPRSS15 HGNC NCBI

Linked Data

dbSNP Id: rs2074688442

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.18280742_18280745del , CM000683.2:g.18280742_18280745del GRCh38
NC_000021.8:g.19653059_19653062del , CM000683.1:g.19653059_19653062del GRCh37
NC_000021.7:g.18574930_18574933del NCBI36
NG_012207.1:g.127911_127914del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284885.8:c.2668+297_2668+300del MANE Select ENSP00000284885.3:n.2668+297_2668+300del
ENST00000284885.7:c.2668+297_2668+300del ENSP00000284885.3:n.2668+297_2668+300del
NM_002772.2:c.2668+297_2668+300del NP_002763.2:n.2668+297_2668+300del
XM_011529654.1:c.2803+297_2803+300del XP_011527956.1:n.2803+297_2803+300del
XM_011529655.1:c.2803+297_2803+300del XP_011527957.1:n.2803+297_2803+300del
XM_011529656.1:c.2803+297_2803+300del XP_011527958.1:n.2803+297_2803+300del
XM_011529657.1:c.2758+297_2758+300del XP_011527959.1:n.2758+297_2758+300del
XM_011529658.1:c.2722+297_2722+300del XP_011527960.1:n.2722+297_2722+300del
XM_011529659.1:c.2713+297_2713+300del XP_011527961.1:n.2713+297_2713+300del
XM_011529654.2:c.2803+297_2803+300del XP_011527956.1:n.2803+297_2803+300del
XM_011529656.2:c.2803+297_2803+300del XP_011527958.1:n.2803+297_2803+300del
XM_011529657.2:c.2758+297_2758+300del XP_011527959.1:n.2758+297_2758+300del
XM_011529658.2:c.2722+297_2722+300del XP_011527960.1:n.2722+297_2722+300del
NM_002772.3:c.2668+297_2668+300del MANE Select NP_002763.3:n.2668+297_2668+300del