Canonical Allele Identifier: CA5852708
Gene: SMPD1 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.907G>C MANE Select ENSP00000340409.4:p.Ala303Pro
ENST00000342245.8:c.907G>C ENSP00000340409.4:p.Ala303Pro
ENST00000526280.1:c.96G>C
ENST00000527275.5:c.904G>C ENSP00000435350.1:p.Ala302Pro
ENST00000530395.1:c.88G>C ENSP00000431479.1:p.Ala30Pro
ENST00000531303.5:c.438+469G>C ENSP00000432625.1:n.438+469G>C
ENST00000533123.5:c.907G>C ENSP00000435950.1:p.Ala303Pro
ENST00000533196.1:n.375-34G>C
ENST00000534405.5:c.907G>C ENSP00000434353.1:p.Ala303Pro
NM_000543.4:c.907G>C NP_000534.3:p.Ala303Pro
NM_001007593.2:c.904G>C NP_001007594.2:p.Ala302Pro
XM_005253075.3:c.907G>C XP_005253132.1:p.Ala303Pro
XM_011520303.1:c.907G>C XP_011518605.1:p.Ala303Pro
XM_011520304.1:c.907G>C XP_011518606.1:p.Ala303Pro
XR_930886.1:n.1205G>C
NM_001318087.1:c.907G>C NP_001305016.1:p.Ala303Pro
NM_001318088.1:c.-55G>C NP_001305017.1:n.-55G>C
NM_001365135.1:c.907G>C NP_001352064.1:p.Ala303Pro
NR_027400.2:n.1092G>C
NR_134502.1:n.623+469G>C
XM_011520304.2:c.907G>C XP_011518606.1:p.Ala303Pro
XR_001747940.2:n.1032G>C
XR_002957158.1:n.1032G>C
NM_000543.5:c.907G>C MANE Select NP_000534.3:p.Ala303Pro
NM_001007593.3:c.904G>C NP_001007594.2:p.Ala302Pro
NM_001318087.2:c.907G>C NP_001305016.1:p.Ala303Pro
NM_001318088.2:c.-55G>C NP_001305017.1:n.-55G>C
NM_001365135.2:c.907G>C NP_001352064.1:p.Ala303Pro
NR_027400.3:n.1032G>C
NR_134502.2:n.563+469G>C