Canonical Allele Identifier: CA667907194
Gene: TSPAN15 HGNC NCBI

Linked Data

dbSNP Id: rs1226810909

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.69503482_69503483del , CM000672.2:g.69503482_69503483del GRCh38
NC_000010.10:g.71263238_71263239del , CM000672.1:g.71263238_71263239del GRCh37
NC_000010.9:g.70933244_70933245del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373290.7:c.571-956_571-955del MANE Select ENSP00000362387.2:n.571-956_571-955del
ENST00000373290.6:c.571-956_571-955del ENSP00000362387.2:n.571-956_571-955del
ENST00000452130.1:c.298-956_298-955del ENSP00000404528.1:n.298-956_298-955del
ENST00000459981.1:n.503-956_503-955del
ENST00000475069.5:n.341-956_341-955del
ENST00000486093.5:n.280-956_280-955del
ENST00000490083.5:n.517-956_517-955del
NM_012339.3:c.571-956_571-955del NP_036471.1:n.571-956_571-955del
XM_005269666.3:c.376-956_376-955del XP_005269723.1:n.376-956_376-955del
XM_005269667.3:c.310-956_310-955del XP_005269724.1:n.310-956_310-955del
XM_006717738.2:c.499-956_499-955del XP_006717801.1:n.499-956_499-955del
XM_011539562.1:c.223-956_223-955del XP_011537864.1:n.223-956_223-955del
XM_011539563.1:c.139-956_139-955del XP_011537865.1:n.139-956_139-955del
XR_945642.1:n.772-956_772-955del
NM_001351263.1:c.310-956_310-955del NP_001338192.1:n.310-956_310-955del
NM_012339.4:c.571-956_571-955del NP_036471.1:n.571-956_571-955del
NR_147091.1:n.770-956_770-955del
XM_005269666.4:c.376-956_376-955del XP_005269723.1:n.376-956_376-955del
XM_011539562.2:c.223-956_223-955del XP_011537864.1:n.223-956_223-955del
XM_011539563.2:c.139-956_139-955del XP_011537865.1:n.139-956_139-955del
XM_017016010.1:c.642-956_642-955del XP_016871499.1:n.642-956_642-955del
XR_001747072.1:n.773-956_773-955del
XR_001747073.1:n.773-956_773-955del
XR_001747074.1:n.699-956_699-955del
NM_012339.5:c.571-956_571-955del MANE Select NP_036471.1:n.571-956_571-955del
NM_001351263.2:c.310-956_310-955del NP_001338192.1:n.310-956_310-955del
NR_147091.2:n.772-956_772-955del