Canonical Allele Identifier: CA379373979
Gene: SMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6393377G>C , CM000673.2:g.6393377G>C GRCh38
NC_000011.9:g.6414607G>C , CM000673.1:g.6414607G>C GRCh37
NC_000011.8:g.6371183G>C NCBI36
NG_011780.1:g.7953G>C
NG_029615.1:g.31038C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.1253G>C MANE Select ENSP00000340409.4:p.Arg418Pro
ENST00000342245.8:c.1253G>C ENSP00000340409.4:p.Arg418Pro
ENST00000526280.1:c.321-240G>C
ENST00000527275.5:c.1250G>C ENSP00000435350.1:p.Arg417Pro
ENST00000531303.5:c.*84G>C ENSP00000432625.1:n.*84G>C
ENST00000531336.1:n.85G>C
ENST00000533123.5:c.1092-240G>C ENSP00000435950.1:n.1092-240G>C
ENST00000534405.5:c.*84G>C ENSP00000434353.1:n.*84G>C
NM_000543.4:c.1253G>C NP_000534.3:p.Arg418Pro
NM_001007593.2:c.1250G>C NP_001007594.2:p.Arg417Pro
XM_005253075.3:c.1253G>C XP_005253132.1:p.Arg418Pro
XM_011520303.1:c.1132-240G>C XP_011518605.1:n.1132-240G>C
XM_011520304.1:c.1132-240G>C XP_011518606.1:n.1132-240G>C
XR_930886.1:n.1591G>C
NM_001318087.1:c.1253G>C NP_001305016.1:p.Arg418Pro
NM_001318088.1:c.332G>C NP_001305017.1:p.Arg111Pro
NM_001365135.1:c.1132-240G>C NP_001352064.1:n.1132-240G>C
NR_027400.2:n.1277-240G>C
NR_134502.1:n.785G>C
XM_011520304.2:c.1132-240G>C XP_011518606.1:n.1132-240G>C
XR_001747940.2:n.1418G>C
XR_002957158.1:n.1418G>C
NM_000543.5:c.1253G>C MANE Select NP_000534.3:p.Arg418Pro
NM_001007593.3:c.1250G>C NP_001007594.2:p.Arg417Pro
NM_001318087.2:c.1253G>C NP_001305016.1:p.Arg418Pro
NM_001318088.2:c.332G>C NP_001305017.1:p.Arg111Pro
NM_001365135.2:c.1132-240G>C NP_001352064.1:n.1132-240G>C
NR_027400.3:n.1217-240G>C
NR_134502.2:n.725G>C