Canonical Allele Identifier: CA1950145512
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390451T= , CM000673.2:g.6390451T= GRCh38
NC_000011.9:g.6411681T= , CM000673.1:g.6411681T= GRCh37
NC_000011.8:g.6368257T= NCBI36
NG_011780.1:g.5027T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.8:c.-148T= ENSP00000340409.4:n.-148T=
ENST00000530395.1:c.-284T= ENSP00000431479.1:n.-284T=
ENST00000533196.1:n.12T=
NM_000543.4:c.-148T= NP_000534.3:n.-148T=
NM_001007593.2:c.-148T= NP_001007594.2:n.-148T=
XM_005253075.3:c.-148T= XP_005253132.1:n.-148T=
XM_011520303.1:c.-148T= XP_011518605.1:n.-148T=
XM_011520304.1:c.-148T= XP_011518606.1:n.-148T=
XR_930886.1:n.151T=
NM_001318087.1:c.-148T= NP_001305016.1:n.-148T=
NM_001318088.1:c.-1109T= NP_001305017.1:n.-1109T=
NR_027400.2:n.38T=
NR_134502.1:n.38T=