Canonical Allele Identifier: CA934768399
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1847979636

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6392515_6392516insTTTTTTG , CM000673.2:g.6392515_6392516insTTTTTTG GRCh38
NC_000011.9:g.6413745_6413746insTTTTTTG , CM000673.1:g.6413745_6413746insTTTTTTG GRCh37
NC_000011.8:g.6370321_6370322insTTTTTTG NCBI36
NG_011780.1:g.7091_7092insTTTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.1091+359_1091+360insTTTTTTG MANE Select ENSP00000340409.4:n.1091+359_1091+360insTTTTTTG
ENST00000342245.8:c.1091+359_1091+360insTTTTTTG ENSP00000340409.4:n.1091+359_1091+360insTTTTTTG
ENST00000526280.1:c.320+319_320+320insTTTTTTG
ENST00000527275.5:c.1088+359_1088+360insTTTTTTG ENSP00000435350.1:n.1088+359_1088+360insTTTTTTG
ENST00000531303.5:c.439-701_439-700insTTTTTTG ENSP00000432625.1:n.439-701_439-700insTTTTTTG
ENST00000533123.5:c.1091+359_1091+360insTTTTTTG ENSP00000435950.1:n.1091+359_1091+360insTTTTTTG
ENST00000534405.5:c.1131+319_1131+320insTTTTTTG ENSP00000434353.1:n.1131+319_1131+320insTTTTTTG
NM_000543.4:c.1091+359_1091+360insTTTTTTG NP_000534.3:n.1091+359_1091+360insTTTTTTG
NM_001007593.2:c.1088+359_1088+360insTTTTTTG NP_001007594.2:n.1088+359_1088+360insTTTTTTG
XM_005253075.3:c.1091+359_1091+360insTTTTTTG XP_005253132.1:n.1091+359_1091+360insTTTTTTG
XM_011520303.1:c.1131+319_1131+320insTTTTTTG XP_011518605.1:n.1131+319_1131+320insTTTTTTG
XM_011520304.1:c.1131+319_1131+320insTTTTTTG XP_011518606.1:n.1131+319_1131+320insTTTTTTG
XR_930886.1:n.1429+319_1429+320insTTTTTTG
NM_001318087.1:c.1091+359_1091+360insTTTTTTG NP_001305016.1:n.1091+359_1091+360insTTTTTTG
NM_001318088.1:c.170+319_170+320insTTTTTTG NP_001305017.1:n.170+319_170+320insTTTTTTG
NM_001365135.1:c.1131+319_1131+320insTTTTTTG NP_001352064.1:n.1131+319_1131+320insTTTTTTG
NR_027400.2:n.1276+359_1276+360insTTTTTTG
NR_134502.1:n.624-701_624-700insTTTTTTG
XM_011520304.2:c.1131+319_1131+320insTTTTTTG XP_011518606.1:n.1131+319_1131+320insTTTTTTG
XR_001747940.2:n.1256+319_1256+320insTTTTTTG
XR_002957158.1:n.1256+319_1256+320insTTTTTTG
NM_000543.5:c.1091+359_1091+360insTTTTTTG MANE Select NP_000534.3:n.1091+359_1091+360insTTTTTTG
NM_001007593.3:c.1088+359_1088+360insTTTTTTG NP_001007594.2:n.1088+359_1088+360insTTTTTTG
NM_001318087.2:c.1091+359_1091+360insTTTTTTG NP_001305016.1:n.1091+359_1091+360insTTTTTTG
NM_001318088.2:c.170+319_170+320insTTTTTTG NP_001305017.1:n.170+319_170+320insTTTTTTG
NM_001365135.2:c.1131+319_1131+320insTTTTTTG NP_001352064.1:n.1131+319_1131+320insTTTTTTG
NR_027400.3:n.1216+359_1216+360insTTTTTTG
NR_134502.2:n.564-701_564-700insTTTTTTG