Canonical Allele Identifier: CA16041475
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 371218
dbSNP Id: rs1057517098

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390791del , CM000673.2:g.6390791del GRCh38
NC_000011.9:g.6412021del , CM000673.1:g.6412021del GRCh37
NC_000011.8:g.6368597del NCBI36
NG_011780.1:g.5367del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.193del MANE Select ENSP00000340409.4:p.Ser65LeufsTer12
ENST00000342245.8:c.193del ENSP00000340409.4:p.Ser65LeufsTer12
ENST00000527275.5:c.193del ENSP00000435350.1:p.Ser65LeufsTer12
ENST00000530395.1:c.-96+152del ENSP00000431479.1:n.-96+152del
ENST00000531303.5:c.193del ENSP00000432625.1:p.Ser65LeufsTer12
ENST00000533123.5:c.193del ENSP00000435950.1:p.Ser65LeufsTer12
ENST00000533196.1:n.352del
ENST00000534405.5:c.193del ENSP00000434353.1:p.Ser65LeufsTer12
NM_000543.4:c.193del NP_000534.3:p.Ser65LeufsTer12
NM_001007593.2:c.193del NP_001007594.2:p.Ser65LeufsTer12
XM_005253075.3:c.193del XP_005253132.1:p.Ser65LeufsTer12
XM_011520303.1:c.193del XP_011518605.1:p.Ser65LeufsTer12
XM_011520304.1:c.193del XP_011518606.1:p.Ser65LeufsTer12
XR_930886.1:n.491del
NM_001318087.1:c.193del NP_001305016.1:p.Ser65LeufsTer12
NM_001318088.1:c.-769del NP_001305017.1:n.-769del
NM_001365135.1:c.193del NP_001352064.1:p.Ser65LeufsTer12
NR_027400.2:n.378del
NR_134502.1:n.378del
XM_011520304.2:c.193del XP_011518606.1:p.Ser65LeufsTer12
XR_001747940.2:n.318del
XR_002957158.1:n.318del
NM_000543.5:c.193del MANE Select NP_000534.3:p.Ser65LeufsTer12
NM_001007593.3:c.193del NP_001007594.2:p.Ser65LeufsTer12
NM_001318087.2:c.193del NP_001305016.1:p.Ser65LeufsTer12
NM_001318088.2:c.-769del NP_001305017.1:n.-769del
NM_001365135.2:c.193del NP_001352064.1:p.Ser65LeufsTer12
NR_027400.3:n.318del
NR_134502.2:n.318del