Canonical Allele Identifier: CA5852551
Gene: SMPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1148131
ClinVar RCV Id: RCV001487861
dbSNP Id: rs747913628
gnomAD v2: 11-6412153-A-T
gnomAD v4: 11-6390923-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390923A>T , CM000673.2:g.6390923A>T GRCh38
NC_000011.9:g.6412153A>T , CM000673.1:g.6412153A>T GRCh37
NC_000011.8:g.6368729A>T NCBI36
NG_011780.1:g.5499A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.318+7A>T MANE Select ENSP00000340409.4:n.318+7A>T
ENST00000342245.8:c.318+7A>T ENSP00000340409.4:n.318+7A>T
ENST00000527275.5:c.318+7A>T ENSP00000435350.1:n.318+7A>T
ENST00000530395.1:c.-96+284A>T ENSP00000431479.1:n.-96+284A>T
ENST00000531303.5:c.318+7A>T ENSP00000432625.1:n.318+7A>T
ENST00000533123.5:c.318+7A>T ENSP00000435950.1:n.318+7A>T
ENST00000533196.1:n.374+110A>T
ENST00000534405.5:c.318+7A>T ENSP00000434353.1:n.318+7A>T
NM_000543.4:c.318+7A>T NP_000534.3:n.318+7A>T
NM_001007593.2:c.318+7A>T NP_001007594.2:n.318+7A>T
XM_005253075.3:c.318+7A>T XP_005253132.1:n.318+7A>T
XM_011520303.1:c.318+7A>T XP_011518605.1:n.318+7A>T
XM_011520304.1:c.318+7A>T XP_011518606.1:n.318+7A>T
XR_930886.1:n.616+7A>T
NM_001318087.1:c.318+7A>T NP_001305016.1:n.318+7A>T
NM_001318088.1:c.-644+7A>T NP_001305017.1:n.-644+7A>T
NM_001365135.1:c.318+7A>T NP_001352064.1:n.318+7A>T
NR_027400.2:n.503+7A>T
NR_134502.1:n.503+7A>T
XM_011520304.2:c.318+7A>T XP_011518606.1:n.318+7A>T
XR_001747940.2:n.443+7A>T
XR_002957158.1:n.443+7A>T
NM_000543.5:c.318+7A>T MANE Select NP_000534.3:n.318+7A>T
NM_001007593.3:c.318+7A>T NP_001007594.2:n.318+7A>T
NM_001318087.2:c.318+7A>T NP_001305016.1:n.318+7A>T
NM_001318088.2:c.-644+7A>T NP_001305017.1:n.-644+7A>T
NM_001365135.2:c.318+7A>T NP_001352064.1:n.318+7A>T
NR_027400.3:n.443+7A>T
NR_134502.2:n.443+7A>T