Canonical Allele Identifier: CA1950147107
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1847980056

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6392516del , CM000673.2:g.6392516del GRCh38
NC_000011.9:g.6413746del , CM000673.1:g.6413746del GRCh37
NC_000011.8:g.6370322del NCBI36
NG_011780.1:g.7092del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.1091+360del MANE Select ENSP00000340409.4:n.1091+360del
ENST00000342245.8:c.1091+360del ENSP00000340409.4:n.1091+360del
ENST00000526280.1:c.320+320del
ENST00000527275.5:c.1088+360del ENSP00000435350.1:n.1088+360del
ENST00000531303.5:c.439-700del ENSP00000432625.1:n.439-700del
ENST00000533123.5:c.1091+360del ENSP00000435950.1:n.1091+360del
ENST00000534405.5:c.1131+320del ENSP00000434353.1:n.1131+320del
NM_000543.4:c.1091+360del NP_000534.3:n.1091+360del
NM_001007593.2:c.1088+360del NP_001007594.2:n.1088+360del
XM_005253075.3:c.1091+360del XP_005253132.1:n.1091+360del
XM_011520303.1:c.1131+320del XP_011518605.1:n.1131+320del
XM_011520304.1:c.1131+320del XP_011518606.1:n.1131+320del
XR_930886.1:n.1429+320del
NM_001318087.1:c.1091+360del NP_001305016.1:n.1091+360del
NM_001318088.1:c.170+320del NP_001305017.1:n.170+320del
NM_001365135.1:c.1131+320del NP_001352064.1:n.1131+320del
NR_027400.2:n.1276+360del
NR_134502.1:n.624-700del
XM_011520304.2:c.1131+320del XP_011518606.1:n.1131+320del
XR_001747940.2:n.1256+320del
XR_002957158.1:n.1256+320del
NM_000543.5:c.1091+360del MANE Select NP_000534.3:n.1091+360del
NM_001007593.3:c.1088+360del NP_001007594.2:n.1088+360del
NM_001318087.2:c.1091+360del NP_001305016.1:n.1091+360del
NM_001318088.2:c.170+320del NP_001305017.1:n.170+320del
NM_001365135.2:c.1131+320del NP_001352064.1:n.1131+320del
NR_027400.3:n.1216+360del
NR_134502.2:n.564-700del