Canonical Allele Identifier: CA1950148379
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6393615A= , CM000673.2:g.6393615A= GRCh38
NC_000011.9:g.6414845A= , CM000673.1:g.6414845A= GRCh37
NC_000011.8:g.6371421A= NCBI36
NG_011780.1:g.8191A=
NG_029615.1:g.30800T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.1264-2A= MANE Select ENSP00000340409.4:n.1264-2A=
ENST00000342245.8:c.1264-2A= ENSP00000340409.4:n.1264-2A=
ENST00000526280.1:c.321-2A=
ENST00000527275.5:c.1261-2A= ENSP00000435350.1:n.1261-2A=
ENST00000531303.5:c.*95-2A= ENSP00000432625.1:n.*95-2A=
ENST00000531336.1:n.96-2A=
ENST00000532367.1:n.98A=
ENST00000533123.5:c.1092-2A= ENSP00000435950.1:n.1092-2A=
ENST00000534405.5:c.*95-2A= ENSP00000434353.1:n.*95-2A=
NM_000543.4:c.1264-2A= NP_000534.3:n.1264-2A=
NM_001007593.2:c.1261-2A= NP_001007594.2:n.1261-2A=
XM_005253075.3:c.1264-2A= XP_005253132.1:n.1264-2A=
XM_011520303.1:c.1132-2A= XP_011518605.1:n.1132-2A=
XM_011520304.1:c.1132-2A= XP_011518606.1:n.1132-2A=
XR_930886.1:n.1602-2A=
NM_001318087.1:c.1264-2A= NP_001305016.1:n.1264-2A=
NM_001318088.1:c.343-2A= NP_001305017.1:n.343-2A=
NM_001365135.1:c.1132-2A= NP_001352064.1:n.1132-2A=
NR_027400.2:n.1277-2A=
NR_134502.1:n.796-2A=
XM_011520304.2:c.1132-2A= XP_011518606.1:n.1132-2A=
XR_001747940.2:n.1429-2A=
XR_002957158.1:n.1429-2A=
NM_000543.5:c.1264-2A= MANE Select NP_000534.3:n.1264-2A=
NM_001007593.3:c.1261-2A= NP_001007594.2:n.1261-2A=
NM_001318087.2:c.1264-2A= NP_001305016.1:n.1264-2A=
NM_001318088.2:c.343-2A= NP_001305017.1:n.343-2A=
NM_001365135.2:c.1132-2A= NP_001352064.1:n.1132-2A=
NR_027400.3:n.1217-2A=
NR_134502.2:n.736-2A=