Canonical Allele Identifier: CA379369858
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 642425
ClinVar RCV Id: RCV000795891
dbSNP Id: rs1215635747

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6391601C>T , CM000673.2:g.6391601C>T GRCh38
NC_000011.9:g.6412831C>T , CM000673.1:g.6412831C>T GRCh37
NC_000011.8:g.6369407C>T NCBI36
NG_011780.1:g.6177C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.536C>T MANE Select ENSP00000340409.4:p.Ser179Phe
ENST00000342245.8:c.536C>T ENSP00000340409.4:p.Ser179Phe
ENST00000527275.5:c.533C>T ENSP00000435350.1:p.Ser178Phe
ENST00000530395.1:c.-95-189C>T ENSP00000431479.1:n.-95-189C>T
ENST00000531303.5:c.438+98C>T ENSP00000432625.1:n.438+98C>T
ENST00000533123.5:c.536C>T ENSP00000435950.1:p.Ser179Phe
ENST00000533196.1:n.375-405C>T
ENST00000534405.5:c.536C>T ENSP00000434353.1:p.Ser179Phe
NM_000543.4:c.536C>T NP_000534.3:p.Ser179Phe
NM_001007593.2:c.533C>T NP_001007594.2:p.Ser178Phe
XM_005253075.3:c.536C>T XP_005253132.1:p.Ser179Phe
XM_011520303.1:c.536C>T XP_011518605.1:p.Ser179Phe
XM_011520304.1:c.536C>T XP_011518606.1:p.Ser179Phe
XR_930886.1:n.834C>T
NM_001318087.1:c.536C>T NP_001305016.1:p.Ser179Phe
NM_001318088.1:c.-426C>T NP_001305017.1:n.-426C>T
NM_001365135.1:c.536C>T NP_001352064.1:p.Ser179Phe
NR_027400.2:n.721C>T
NR_134502.1:n.623+98C>T
XM_011520304.2:c.536C>T XP_011518606.1:p.Ser179Phe
XR_001747940.2:n.661C>T
XR_002957158.1:n.661C>T
NM_000543.5:c.536C>T MANE Select NP_000534.3:p.Ser179Phe
NM_001007593.3:c.533C>T NP_001007594.2:p.Ser178Phe
NM_001318087.2:c.536C>T NP_001305016.1:p.Ser179Phe
NM_001318088.2:c.-426C>T NP_001305017.1:n.-426C>T
NM_001365135.2:c.536C>T NP_001352064.1:p.Ser179Phe
NR_027400.3:n.661C>T
NR_134502.2:n.563+98C>T