Canonical Allele Identifier: CA379374440
Gene: SMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6393665A>C , CM000673.2:g.6393665A>C GRCh38
NC_000011.9:g.6414895A>C , CM000673.1:g.6414895A>C GRCh37
NC_000011.8:g.6371471A>C NCBI36
NG_011780.1:g.8241A>C
NG_029615.1:g.30750T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.1312A>C MANE Select ENSP00000340409.4:p.Ser438Arg
ENST00000342245.8:c.1312A>C ENSP00000340409.4:p.Ser438Arg
ENST00000526280.1:c.369A>C
ENST00000527275.5:c.1309A>C ENSP00000435350.1:p.Ser437Arg
ENST00000531303.5:c.*143A>C ENSP00000432625.1:n.*143A>C
ENST00000531336.1:n.144A>C
ENST00000532367.1:n.148A>C
ENST00000533123.5:c.*39A>C ENSP00000435950.1:n.*39A>C
ENST00000534405.5:c.*143A>C ENSP00000434353.1:n.*143A>C
NM_000543.4:c.1312A>C NP_000534.3:p.Ser438Arg
NM_001007593.2:c.1309A>C NP_001007594.2:p.Ser437Arg
XM_005253075.3:c.1312A>C XP_005253132.1:p.Ser438Arg
XM_011520303.1:c.1180A>C XP_011518605.1:p.Ser394Arg
XM_011520304.1:c.1180A>C XP_011518606.1:p.Ser394Arg
XR_930886.1:n.1650A>C
NM_001318087.1:c.1312A>C NP_001305016.1:p.Ser438Arg
NM_001318088.1:c.391A>C NP_001305017.1:p.Ser131Arg
NM_001365135.1:c.1180A>C NP_001352064.1:p.Ser394Arg
NR_027400.2:n.1325A>C
NR_134502.1:n.844A>C
XM_011520304.2:c.1180A>C XP_011518606.1:p.Ser394Arg
XR_001747940.2:n.1477A>C
XR_002957158.1:n.1477A>C
NM_000543.5:c.1312A>C MANE Select NP_000534.3:p.Ser438Arg
NM_001007593.3:c.1309A>C NP_001007594.2:p.Ser437Arg
NM_001318087.2:c.1312A>C NP_001305016.1:p.Ser438Arg
NM_001318088.2:c.391A>C NP_001305017.1:p.Ser131Arg
NM_001365135.2:c.1180A>C NP_001352064.1:p.Ser394Arg
NR_027400.3:n.1265A>C
NR_134502.2:n.784A>C