Canonical Allele Identifier: CA5852724
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 403463
dbSNP Id: rs202081954
gnomAD v2: 11-6413290-C-G
gnomAD v3: 11-6392060-C-G
gnomAD v4: 11-6392060-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6392060C>G , CM000673.2:g.6392060C>G GRCh38
NC_000011.9:g.6413290C>G , CM000673.1:g.6413290C>G GRCh37
NC_000011.8:g.6369866C>G NCBI36
NG_011780.1:g.6636C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.995C>G MANE Select ENSP00000340409.4:p.Pro332Arg
ENST00000342245.8:c.995C>G ENSP00000340409.4:p.Pro332Arg
ENST00000526280.1:c.184C>G
ENST00000527275.5:c.992C>G ENSP00000435350.1:p.Pro331Arg
ENST00000531303.5:c.438+557C>G ENSP00000432625.1:n.438+557C>G
ENST00000533123.5:c.995C>G ENSP00000435950.1:p.Pro332Arg
ENST00000534405.5:c.995C>G ENSP00000434353.1:p.Pro332Arg
NM_000543.4:c.995C>G NP_000534.3:p.Pro332Arg
NM_001007593.2:c.992C>G NP_001007594.2:p.Pro331Arg
XM_005253075.3:c.995C>G XP_005253132.1:p.Pro332Arg
XM_011520303.1:c.995C>G XP_011518605.1:p.Pro332Arg
XM_011520304.1:c.995C>G XP_011518606.1:p.Pro332Arg
XR_930886.1:n.1293C>G
NM_001318087.1:c.995C>G NP_001305016.1:p.Pro332Arg
NM_001318088.1:c.34C>G NP_001305017.1:p.Pro12Ala
NM_001365135.1:c.995C>G NP_001352064.1:p.Pro332Arg
NR_027400.2:n.1180C>G
NR_134502.1:n.623+557C>G
XM_011520304.2:c.995C>G XP_011518606.1:p.Pro332Arg
XR_001747940.2:n.1120C>G
XR_002957158.1:n.1120C>G
NM_000543.5:c.995C>G MANE Select NP_000534.3:p.Pro332Arg
NM_001007593.3:c.992C>G NP_001007594.2:p.Pro331Arg
NM_001318087.2:c.995C>G NP_001305016.1:p.Pro332Arg
NM_001318088.2:c.34C>G NP_001305017.1:p.Pro12Ala
NM_001365135.2:c.995C>G NP_001352064.1:p.Pro332Arg
NR_027400.3:n.1120C>G
NR_134502.2:n.563+557C>G