Canonical Allele Identifier: CA679152318
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1311020167

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6392508_6392509insG , CM000673.2:g.6392508_6392509insG GRCh38
NC_000011.9:g.6413738_6413739insG , CM000673.1:g.6413738_6413739insG GRCh37
NC_000011.8:g.6370314_6370315insG NCBI36
NG_011780.1:g.7084_7085insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.1091+352_1091+353insG MANE Select ENSP00000340409.4:n.1091+352_1091+353insG
ENST00000342245.8:c.1091+352_1091+353insG ENSP00000340409.4:n.1091+352_1091+353insG
ENST00000526280.1:c.320+312_320+313insG
ENST00000527275.5:c.1088+352_1088+353insG ENSP00000435350.1:n.1088+352_1088+353insG
ENST00000531303.5:c.439-708_439-707insG ENSP00000432625.1:n.439-708_439-707insG
ENST00000533123.5:c.1091+352_1091+353insG ENSP00000435950.1:n.1091+352_1091+353insG
ENST00000534405.5:c.1131+312_1131+313insG ENSP00000434353.1:n.1131+312_1131+313insG
NM_000543.4:c.1091+352_1091+353insG NP_000534.3:n.1091+352_1091+353insG
NM_001007593.2:c.1088+352_1088+353insG NP_001007594.2:n.1088+352_1088+353insG
XM_005253075.3:c.1091+352_1091+353insG XP_005253132.1:n.1091+352_1091+353insG
XM_011520303.1:c.1131+312_1131+313insG XP_011518605.1:n.1131+312_1131+313insG
XM_011520304.1:c.1131+312_1131+313insG XP_011518606.1:n.1131+312_1131+313insG
XR_930886.1:n.1429+312_1429+313insG
NM_001318087.1:c.1091+352_1091+353insG NP_001305016.1:n.1091+352_1091+353insG
NM_001318088.1:c.170+312_170+313insG NP_001305017.1:n.170+312_170+313insG
NM_001365135.1:c.1131+312_1131+313insG NP_001352064.1:n.1131+312_1131+313insG
NR_027400.2:n.1276+352_1276+353insG
NR_134502.1:n.624-708_624-707insG
XM_011520304.2:c.1131+312_1131+313insG XP_011518606.1:n.1131+312_1131+313insG
XR_001747940.2:n.1256+312_1256+313insG
XR_002957158.1:n.1256+312_1256+313insG
NM_000543.5:c.1091+352_1091+353insG MANE Select NP_000534.3:n.1091+352_1091+353insG
NM_001007593.3:c.1088+352_1088+353insG NP_001007594.2:n.1088+352_1088+353insG
NM_001318087.2:c.1091+352_1091+353insG NP_001305016.1:n.1091+352_1091+353insG
NM_001318088.2:c.170+312_170+313insG NP_001305017.1:n.170+312_170+313insG
NM_001365135.2:c.1131+312_1131+313insG NP_001352064.1:n.1131+312_1131+313insG
NR_027400.3:n.1216+352_1216+353insG
NR_134502.2:n.564-708_564-707insG