Canonical Allele Identifier: CA1950148258
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6393482G= , CM000673.2:g.6393482G= GRCh38
NC_000011.9:g.6414712G= , CM000673.1:g.6414712G= GRCh37
NC_000011.8:g.6371288G= NCBI36
NG_011780.1:g.8058G=
NG_029615.1:g.30933C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.1263+95G= MANE Select ENSP00000340409.4:n.1263+95G=
ENST00000342245.8:c.1263+95G= ENSP00000340409.4:n.1263+95G=
ENST00000526280.1:c.321-135G=
ENST00000527275.5:c.1260+95G= ENSP00000435350.1:n.1260+95G=
ENST00000531303.5:c.*94+95G= ENSP00000432625.1:n.*94+95G=
ENST00000531336.1:n.95+95G=
ENST00000533123.5:c.1092-135G= ENSP00000435950.1:n.1092-135G=
ENST00000534405.5:c.*94+95G= ENSP00000434353.1:n.*94+95G=
NM_000543.4:c.1263+95G= NP_000534.3:n.1263+95G=
NM_001007593.2:c.1260+95G= NP_001007594.2:n.1260+95G=
XM_005253075.3:c.1263+95G= XP_005253132.1:n.1263+95G=
XM_011520303.1:c.1132-135G= XP_011518605.1:n.1132-135G=
XM_011520304.1:c.1132-135G= XP_011518606.1:n.1132-135G=
XR_930886.1:n.1601+95G=
NM_001318087.1:c.1263+95G= NP_001305016.1:n.1263+95G=
NM_001318088.1:c.342+95G= NP_001305017.1:n.342+95G=
NM_001365135.1:c.1132-135G= NP_001352064.1:n.1132-135G=
NR_027400.2:n.1277-135G=
NR_134502.1:n.795+95G=
XM_011520304.2:c.1132-135G= XP_011518606.1:n.1132-135G=
XR_001747940.2:n.1428+95G=
XR_002957158.1:n.1428+95G=
NM_000543.5:c.1263+95G= MANE Select NP_000534.3:n.1263+95G=
NM_001007593.3:c.1260+95G= NP_001007594.2:n.1260+95G=
NM_001318087.2:c.1263+95G= NP_001305016.1:n.1263+95G=
NM_001318088.2:c.342+95G= NP_001305017.1:n.342+95G=
NM_001365135.2:c.1132-135G= NP_001352064.1:n.1132-135G=
NR_027400.3:n.1217-135G=
NR_134502.2:n.735+95G=