Canonical Allele Identifier: CA379371281
Gene: SMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6391985A>G , CM000673.2:g.6391985A>G GRCh38
NC_000011.9:g.6413215A>G , CM000673.1:g.6413215A>G GRCh37
NC_000011.8:g.6369791A>G NCBI36
NG_011780.1:g.6561A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.920A>G MANE Select ENSP00000340409.4:p.Lys307Arg
ENST00000342245.8:c.920A>G ENSP00000340409.4:p.Lys307Arg
ENST00000526280.1:c.109A>G
ENST00000527275.5:c.917A>G ENSP00000435350.1:p.Lys306Arg
ENST00000530395.1:c.101A>G ENSP00000431479.1:p.Lys34Arg
ENST00000531303.5:c.438+482A>G ENSP00000432625.1:n.438+482A>G
ENST00000533123.5:c.920A>G ENSP00000435950.1:p.Lys307Arg
ENST00000533196.1:n.375-21A>G
ENST00000534405.5:c.920A>G ENSP00000434353.1:p.Lys307Arg
NM_000543.4:c.920A>G NP_000534.3:p.Lys307Arg
NM_001007593.2:c.917A>G NP_001007594.2:p.Lys306Arg
XM_005253075.3:c.920A>G XP_005253132.1:p.Lys307Arg
XM_011520303.1:c.920A>G XP_011518605.1:p.Lys307Arg
XM_011520304.1:c.920A>G XP_011518606.1:p.Lys307Arg
XR_930886.1:n.1218A>G
NM_001318087.1:c.920A>G NP_001305016.1:p.Lys307Arg
NM_001318088.1:c.-42A>G NP_001305017.1:n.-42A>G
NM_001365135.1:c.920A>G NP_001352064.1:p.Lys307Arg
NR_027400.2:n.1105A>G
NR_134502.1:n.623+482A>G
XM_011520304.2:c.920A>G XP_011518606.1:p.Lys307Arg
XR_001747940.2:n.1045A>G
XR_002957158.1:n.1045A>G
NM_000543.5:c.920A>G MANE Select NP_000534.3:p.Lys307Arg
NM_001007593.3:c.917A>G NP_001007594.2:p.Lys306Arg
NM_001318087.2:c.920A>G NP_001305016.1:p.Lys307Arg
NM_001318088.2:c.-42A>G NP_001305017.1:n.-42A>G
NM_001365135.2:c.920A>G NP_001352064.1:p.Lys307Arg
NR_027400.3:n.1045A>G
NR_134502.2:n.563+482A>G