Canonical Allele Identifier: CA1950146310
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6391757G= , CM000673.2:g.6391757G= GRCh38
NC_000011.9:g.6412987G= , CM000673.1:g.6412987G= GRCh37
NC_000011.8:g.6369563G= NCBI36
NG_011780.1:g.6333G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.692G= MANE Select ENSP00000340409.4:p.Arg231=
ENST00000342245.8:c.692G= ENSP00000340409.4:p.Arg231=
ENST00000527275.5:c.689G= ENSP00000435350.1:p.Arg230=
ENST00000530395.1:c.-95-33G= ENSP00000431479.1:n.-95-33G=
ENST00000531303.5:c.438+254G= ENSP00000432625.1:n.438+254G=
ENST00000533123.5:c.692G= ENSP00000435950.1:p.Arg231=
ENST00000533196.1:n.375-249G=
ENST00000534405.5:c.692G= ENSP00000434353.1:p.Arg231=
NM_000543.4:c.692G= NP_000534.3:p.Arg231=
NM_001007593.2:c.689G= NP_001007594.2:p.Arg230=
XM_005253075.3:c.692G= XP_005253132.1:p.Arg231=
XM_011520303.1:c.692G= XP_011518605.1:p.Arg231=
XM_011520304.1:c.692G= XP_011518606.1:p.Arg231=
XR_930886.1:n.990G=
NM_001318087.1:c.692G= NP_001305016.1:p.Arg231=
NM_001318088.1:c.-270G= NP_001305017.1:n.-270G=
NM_001365135.1:c.692G= NP_001352064.1:p.Arg231=
NR_027400.2:n.877G=
NR_134502.1:n.623+254G=
XM_011520304.2:c.692G= XP_011518606.1:p.Arg231=
XR_001747940.2:n.817G=
XR_002957158.1:n.817G=
NM_000543.5:c.692G= MANE Select NP_000534.3:p.Arg231=
NM_001007593.3:c.689G= NP_001007594.2:p.Arg230=
NM_001318087.2:c.692G= NP_001305016.1:p.Arg231=
NM_001318088.2:c.-270G= NP_001305017.1:n.-270G=
NM_001365135.2:c.692G= NP_001352064.1:p.Arg231=
NR_027400.3:n.817G=
NR_134502.2:n.563+254G=