Canonical Allele Identifier: CA1950146474
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6392059C= , CM000673.2:g.6392059C= GRCh38
NC_000011.9:g.6413289C= , CM000673.1:g.6413289C= GRCh37
NC_000011.8:g.6369865C= NCBI36
NG_011780.1:g.6635C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.994C= MANE Select ENSP00000340409.4:p.Pro332=
ENST00000342245.8:c.994C= ENSP00000340409.4:p.Pro332=
ENST00000526280.1:c.183C=
ENST00000527275.5:c.991C= ENSP00000435350.1:p.Pro331=
ENST00000531303.5:c.438+556C= ENSP00000432625.1:n.438+556C=
ENST00000533123.5:c.994C= ENSP00000435950.1:p.Pro332=
ENST00000534405.5:c.994C= ENSP00000434353.1:p.Pro332=
NM_000543.4:c.994C= NP_000534.3:p.Pro332=
NM_001007593.2:c.991C= NP_001007594.2:p.Pro331=
XM_005253075.3:c.994C= XP_005253132.1:p.Pro332=
XM_011520303.1:c.994C= XP_011518605.1:p.Pro332=
XM_011520304.1:c.994C= XP_011518606.1:p.Pro332=
XR_930886.1:n.1292C=
NM_001318087.1:c.994C= NP_001305016.1:p.Pro332=
NM_001318088.1:c.33C= NP_001305017.1:p.Pro11=
NM_001365135.1:c.994C= NP_001352064.1:p.Pro332=
NR_027400.2:n.1179C=
NR_134502.1:n.623+556C=
XM_011520304.2:c.994C= XP_011518606.1:p.Pro332=
XR_001747940.2:n.1119C=
XR_002957158.1:n.1119C=
NM_000543.5:c.994C= MANE Select NP_000534.3:p.Pro332=
NM_001007593.3:c.991C= NP_001007594.2:p.Pro331=
NM_001318087.2:c.994C= NP_001305016.1:p.Pro332=
NM_001318088.2:c.33C= NP_001305017.1:p.Pro11=
NM_001365135.2:c.994C= NP_001352064.1:p.Pro332=
NR_027400.3:n.1119C=
NR_134502.2:n.563+556C=