Canonical Allele Identifier: CA1950147674
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6393176T= , CM000673.2:g.6393176T= GRCh38
NC_000011.9:g.6414406T= , CM000673.1:g.6414406T= GRCh37
NC_000011.8:g.6370982T= NCBI36
NG_011780.1:g.7752T=
NG_029615.1:g.31239A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.1092-40T= MANE Select ENSP00000340409.4:n.1092-40T=
ENST00000342245.8:c.1092-40T= ENSP00000340409.4:n.1092-40T=
ENST00000526280.1:c.321-441T=
ENST00000527275.5:c.1089-40T= ENSP00000435350.1:n.1089-40T=
ENST00000531303.5:c.439-40T= ENSP00000432625.1:n.439-40T=
ENST00000533123.5:c.1092-441T= ENSP00000435950.1:n.1092-441T=
ENST00000534405.5:c.1132-40T= ENSP00000434353.1:n.1132-40T=
NM_000543.4:c.1092-40T= NP_000534.3:n.1092-40T=
NM_001007593.2:c.1089-40T= NP_001007594.2:n.1089-40T=
XM_005253075.3:c.1092-40T= XP_005253132.1:n.1092-40T=
XM_011520303.1:c.1132-441T= XP_011518605.1:n.1132-441T=
XM_011520304.1:c.1132-441T= XP_011518606.1:n.1132-441T=
XR_930886.1:n.1430-40T=
NM_001318087.1:c.1092-40T= NP_001305016.1:n.1092-40T=
NM_001318088.1:c.171-40T= NP_001305017.1:n.171-40T=
NM_001365135.1:c.1132-441T= NP_001352064.1:n.1132-441T=
NR_027400.2:n.1277-441T=
NR_134502.1:n.624-40T=
XM_011520304.2:c.1132-441T= XP_011518606.1:n.1132-441T=
XR_001747940.2:n.1257-40T=
XR_002957158.1:n.1257-40T=
NM_000543.5:c.1092-40T= MANE Select NP_000534.3:n.1092-40T=
NM_001007593.3:c.1089-40T= NP_001007594.2:n.1089-40T=
NM_001318087.2:c.1092-40T= NP_001305016.1:n.1092-40T=
NM_001318088.2:c.171-40T= NP_001305017.1:n.171-40T=
NM_001365135.2:c.1132-441T= NP_001352064.1:n.1132-441T=
NR_027400.3:n.1217-441T=
NR_134502.2:n.564-40T=