Canonical Allele Identifier: CA5852707
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs570353618
gnomAD v2: 11-6413202-G-A
gnomAD v3: 11-6391972-G-A
gnomAD v4: 11-6391972-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6391972G>A , CM000673.2:g.6391972G>A GRCh38
NC_000011.9:g.6413202G>A , CM000673.1:g.6413202G>A GRCh37
NC_000011.8:g.6369778G>A NCBI36
NG_011780.1:g.6548G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.907G>A MANE Select ENSP00000340409.4:p.Ala303Thr
ENST00000342245.8:c.907G>A ENSP00000340409.4:p.Ala303Thr
ENST00000526280.1:c.96G>A
ENST00000527275.5:c.904G>A ENSP00000435350.1:p.Ala302Thr
ENST00000530395.1:c.88G>A ENSP00000431479.1:p.Ala30Thr
ENST00000531303.5:c.438+469G>A ENSP00000432625.1:n.438+469G>A
ENST00000533123.5:c.907G>A ENSP00000435950.1:p.Ala303Thr
ENST00000533196.1:n.375-34G>A
ENST00000534405.5:c.907G>A ENSP00000434353.1:p.Ala303Thr
NM_000543.4:c.907G>A NP_000534.3:p.Ala303Thr
NM_001007593.2:c.904G>A NP_001007594.2:p.Ala302Thr
XM_005253075.3:c.907G>A XP_005253132.1:p.Ala303Thr
XM_011520303.1:c.907G>A XP_011518605.1:p.Ala303Thr
XM_011520304.1:c.907G>A XP_011518606.1:p.Ala303Thr
XR_930886.1:n.1205G>A
NM_001318087.1:c.907G>A NP_001305016.1:p.Ala303Thr
NM_001318088.1:c.-55G>A NP_001305017.1:n.-55G>A
NM_001365135.1:c.907G>A NP_001352064.1:p.Ala303Thr
NR_027400.2:n.1092G>A
NR_134502.1:n.623+469G>A
XM_011520304.2:c.907G>A XP_011518606.1:p.Ala303Thr
XR_001747940.2:n.1032G>A
XR_002957158.1:n.1032G>A
NM_000543.5:c.907G>A MANE Select NP_000534.3:p.Ala303Thr
NM_001007593.3:c.904G>A NP_001007594.2:p.Ala302Thr
NM_001318087.2:c.907G>A NP_001305016.1:p.Ala303Thr
NM_001318088.2:c.-55G>A NP_001305017.1:n.-55G>A
NM_001365135.2:c.907G>A NP_001352064.1:p.Ala303Thr
NR_027400.3:n.1032G>A
NR_134502.2:n.563+469G>A