Canonical Allele Identifier: CA1950146503
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6392077C= , CM000673.2:g.6392077C= GRCh38
NC_000011.9:g.6413307C= , CM000673.1:g.6413307C= GRCh37
NC_000011.8:g.6369883C= NCBI36
NG_011780.1:g.6653C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.1012C= MANE Select ENSP00000340409.4:p.His338=
ENST00000342245.8:c.1012C= ENSP00000340409.4:p.His338=
ENST00000526280.1:c.201C=
ENST00000527275.5:c.1009C= ENSP00000435350.1:p.His337=
ENST00000531303.5:c.438+574C= ENSP00000432625.1:n.438+574C=
ENST00000533123.5:c.1012C= ENSP00000435950.1:p.His338=
ENST00000534405.5:c.1012C= ENSP00000434353.1:p.His338=
NM_000543.4:c.1012C= NP_000534.3:p.His338=
NM_001007593.2:c.1009C= NP_001007594.2:p.His337=
XM_005253075.3:c.1012C= XP_005253132.1:p.His338=
XM_011520303.1:c.1012C= XP_011518605.1:p.His338=
XM_011520304.1:c.1012C= XP_011518606.1:p.His338=
XR_930886.1:n.1310C=
NM_001318087.1:c.1012C= NP_001305016.1:p.His338=
NM_001318088.1:c.51C= NP_001305017.1:p.Thr17=
NM_001365135.1:c.1012C= NP_001352064.1:p.His338=
NR_027400.2:n.1197C=
NR_134502.1:n.623+574C=
XM_011520304.2:c.1012C= XP_011518606.1:p.His338=
XR_001747940.2:n.1137C=
XR_002957158.1:n.1137C=
NM_000543.5:c.1012C= MANE Select NP_000534.3:p.His338=
NM_001007593.3:c.1009C= NP_001007594.2:p.His337=
NM_001318087.2:c.1012C= NP_001305016.1:p.His338=
NM_001318088.2:c.51C= NP_001305017.1:p.Thr17=
NM_001365135.2:c.1012C= NP_001352064.1:p.His338=
NR_027400.3:n.1137C=
NR_134502.2:n.563+574C=