Canonical Allele Identifier: CA5852481
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs781742000

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390704_6390713del , CM000673.2:g.6390704_6390713del GRCh38
NC_000011.9:g.6411934_6411943del , CM000673.1:g.6411934_6411943del GRCh37
NC_000011.8:g.6368510_6368519del NCBI36
NG_011780.1:g.5280_5289del

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.106_115del MANE Select ENSP00000340409.4:p.Val36TrpfsTer?
ENST00000342245.8:c.106_115del ENSP00000340409.4:p.Val36TrpfsTer?
ENST00000527275.5:c.106_115del ENSP00000435350.1:p.Val36TrpfsTer?
ENST00000530395.1:c.-96+65_-96+74del ENSP00000431479.1:n.-96+65_-96+74del
ENST00000531303.5:c.106_115del ENSP00000432625.1:p.Val36TrpfsTer?
ENST00000533123.5:c.106_115del ENSP00000435950.1:p.Val36TrpfsTer?
ENST00000533196.1:n.265_274del
ENST00000534405.5:c.106_115del ENSP00000434353.1:p.Val36TrpfsTer?
NM_000543.4:c.106_115del NP_000534.3:p.Val36TrpfsTer?
NM_001007593.2:c.106_115del NP_001007594.2:p.Val36TrpfsTer?
XM_005253075.3:c.106_115del XP_005253132.1:p.Val36TrpfsTer?
XM_011520303.1:c.106_115del XP_011518605.1:p.Val36TrpfsTer?
XM_011520304.1:c.106_115del XP_011518606.1:p.Val36TrpfsTer?
XR_930886.1:n.404_413del
NM_001318087.1:c.106_115del NP_001305016.1:p.Val36TrpfsTer?
NM_001318088.1:c.-856_-847del NP_001305017.1:n.-856_-847del
NM_001365135.1:c.106_115del NP_001352064.1:p.Val36TrpfsTer?
NR_027400.2:n.291_300del
NR_134502.1:n.291_300del
XM_011520304.2:c.106_115del XP_011518606.1:p.Val36TrpfsTer?
XR_001747940.2:n.231_240del
XR_002957158.1:n.231_240del
NM_000543.5:c.106_115del MANE Select NP_000534.3:p.Val36TrpfsTer?
NM_001007593.3:c.106_115del NP_001007594.2:p.Val36TrpfsTer?
NM_001318087.2:c.106_115del NP_001305016.1:p.Val36TrpfsTer?
NM_001318088.2:c.-856_-847del NP_001305017.1:n.-856_-847del
NM_001365135.2:c.106_115del NP_001352064.1:p.Val36TrpfsTer?
NR_027400.3:n.231_240del
NR_134502.2:n.231_240del