Canonical Allele Identifier: CA934767916
Gene: SMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6392364_6392365insTTT , CM000673.2:g.6392364_6392365insTTT GRCh38
NC_000011.9:g.6413594_6413595insTTT , CM000673.1:g.6413594_6413595insTTT GRCh37
NC_000011.8:g.6370170_6370171insTTT NCBI36
NG_011780.1:g.6940_6941insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.1091+208_1091+209insTTT MANE Select ENSP00000340409.4:n.1091+208_1091+209insTTT
ENST00000342245.8:c.1091+208_1091+209insTTT ENSP00000340409.4:n.1091+208_1091+209insTTT
ENST00000526280.1:c.320+168_320+169insTTT
ENST00000527275.5:c.1088+208_1088+209insTTT ENSP00000435350.1:n.1088+208_1088+209insTTT
ENST00000531303.5:c.439-852_439-851insTTT ENSP00000432625.1:n.439-852_439-851insTTT
ENST00000533123.5:c.1091+208_1091+209insTTT ENSP00000435950.1:n.1091+208_1091+209insTTT
ENST00000534405.5:c.1131+168_1131+169insTTT ENSP00000434353.1:n.1131+168_1131+169insTTT
NM_000543.4:c.1091+208_1091+209insTTT NP_000534.3:n.1091+208_1091+209insTTT
NM_001007593.2:c.1088+208_1088+209insTTT NP_001007594.2:n.1088+208_1088+209insTTT
XM_005253075.3:c.1091+208_1091+209insTTT XP_005253132.1:n.1091+208_1091+209insTTT
XM_011520303.1:c.1131+168_1131+169insTTT XP_011518605.1:n.1131+168_1131+169insTTT
XM_011520304.1:c.1131+168_1131+169insTTT XP_011518606.1:n.1131+168_1131+169insTTT
XR_930886.1:n.1429+168_1429+169insTTT
NM_001318087.1:c.1091+208_1091+209insTTT NP_001305016.1:n.1091+208_1091+209insTTT
NM_001318088.1:c.170+168_170+169insTTT NP_001305017.1:n.170+168_170+169insTTT
NM_001365135.1:c.1131+168_1131+169insTTT NP_001352064.1:n.1131+168_1131+169insTTT
NR_027400.2:n.1276+208_1276+209insTTT
NR_134502.1:n.624-852_624-851insTTT
XM_011520304.2:c.1131+168_1131+169insTTT XP_011518606.1:n.1131+168_1131+169insTTT
XR_001747940.2:n.1256+168_1256+169insTTT
XR_002957158.1:n.1256+168_1256+169insTTT
NM_000543.5:c.1091+208_1091+209insTTT MANE Select NP_000534.3:n.1091+208_1091+209insTTT
NM_001007593.3:c.1088+208_1088+209insTTT NP_001007594.2:n.1088+208_1088+209insTTT
NM_001318087.2:c.1091+208_1091+209insTTT NP_001305016.1:n.1091+208_1091+209insTTT
NM_001318088.2:c.170+168_170+169insTTT NP_001305017.1:n.170+168_170+169insTTT
NM_001365135.2:c.1131+168_1131+169insTTT NP_001352064.1:n.1131+168_1131+169insTTT
NR_027400.3:n.1216+208_1216+209insTTT
NR_134502.2:n.564-852_564-851insTTT