Canonical Allele Identifier: CA379371489
Gene: SMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6392047A>G , CM000673.2:g.6392047A>G GRCh38
NC_000011.9:g.6413277A>G , CM000673.1:g.6413277A>G GRCh37
NC_000011.8:g.6369853A>G NCBI36
NG_011780.1:g.6623A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.982A>G MANE Select ENSP00000340409.4:p.Ser328Gly
ENST00000342245.8:c.982A>G ENSP00000340409.4:p.Ser328Gly
ENST00000526280.1:c.171A>G
ENST00000527275.5:c.979A>G ENSP00000435350.1:p.Ser327Gly
ENST00000531303.5:c.438+544A>G ENSP00000432625.1:n.438+544A>G
ENST00000533123.5:c.982A>G ENSP00000435950.1:p.Ser328Gly
ENST00000533196.1:n.416A>G
ENST00000534405.5:c.982A>G ENSP00000434353.1:p.Ser328Gly
NM_000543.4:c.982A>G NP_000534.3:p.Ser328Gly
NM_001007593.2:c.979A>G NP_001007594.2:p.Ser327Gly
XM_005253075.3:c.982A>G XP_005253132.1:p.Ser328Gly
XM_011520303.1:c.982A>G XP_011518605.1:p.Ser328Gly
XM_011520304.1:c.982A>G XP_011518606.1:p.Ser328Gly
XR_930886.1:n.1280A>G
NM_001318087.1:c.982A>G NP_001305016.1:p.Ser328Gly
NM_001318088.1:c.21A>G NP_001305017.1:p.Ile7Met
NM_001365135.1:c.982A>G NP_001352064.1:p.Ser328Gly
NR_027400.2:n.1167A>G
NR_134502.1:n.623+544A>G
XM_011520304.2:c.982A>G XP_011518606.1:p.Ser328Gly
XR_001747940.2:n.1107A>G
XR_002957158.1:n.1107A>G
NM_000543.5:c.982A>G MANE Select NP_000534.3:p.Ser328Gly
NM_001007593.3:c.979A>G NP_001007594.2:p.Ser327Gly
NM_001318087.2:c.982A>G NP_001305016.1:p.Ser328Gly
NM_001318088.2:c.21A>G NP_001305017.1:p.Ile7Met
NM_001365135.2:c.982A>G NP_001352064.1:p.Ser328Gly
NR_027400.3:n.1107A>G
NR_134502.2:n.563+544A>G