Canonical Allele Identifier: CA1950147536
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1590742964

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6393028C>T , CM000673.2:g.6393028C>T GRCh38
NC_000011.9:g.6414258C>T , CM000673.1:g.6414258C>T GRCh37
NC_000011.8:g.6370834C>T NCBI36
NG_011780.1:g.7604C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.1092-188C>T MANE Select ENSP00000340409.4:n.1092-188C>T
ENST00000342245.8:c.1092-188C>T ENSP00000340409.4:n.1092-188C>T
ENST00000526280.1:c.321-589C>T
ENST00000527275.5:c.1089-188C>T ENSP00000435350.1:n.1089-188C>T
ENST00000531303.5:c.439-188C>T ENSP00000432625.1:n.439-188C>T
ENST00000533123.5:c.1092-589C>T ENSP00000435950.1:n.1092-589C>T
ENST00000534405.5:c.1132-188C>T ENSP00000434353.1:n.1132-188C>T
NM_000543.4:c.1092-188C>T NP_000534.3:n.1092-188C>T
NM_001007593.2:c.1089-188C>T NP_001007594.2:n.1089-188C>T
XM_005253075.3:c.1092-188C>T XP_005253132.1:n.1092-188C>T
XM_011520303.1:c.1132-589C>T XP_011518605.1:n.1132-589C>T
XM_011520304.1:c.1132-589C>T XP_011518606.1:n.1132-589C>T
XR_930886.1:n.1430-188C>T
NM_001318087.1:c.1092-188C>T NP_001305016.1:n.1092-188C>T
NM_001318088.1:c.171-188C>T NP_001305017.1:n.171-188C>T
NM_001365135.1:c.1132-589C>T NP_001352064.1:n.1132-589C>T
NR_027400.2:n.1277-589C>T
NR_134502.1:n.624-188C>T
XM_011520304.2:c.1132-589C>T XP_011518606.1:n.1132-589C>T
XR_001747940.2:n.1257-188C>T
XR_002957158.1:n.1257-188C>T
NM_000543.5:c.1092-188C>T MANE Select NP_000534.3:n.1092-188C>T
NM_001007593.3:c.1089-188C>T NP_001007594.2:n.1089-188C>T
NM_001318087.2:c.1092-188C>T NP_001305016.1:n.1092-188C>T
NM_001318088.2:c.171-188C>T NP_001305017.1:n.171-188C>T
NM_001365135.2:c.1132-589C>T NP_001352064.1:n.1132-589C>T
NR_027400.3:n.1217-589C>T
NR_134502.2:n.564-188C>T