Canonical Allele Identifier: CA934769846
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1848122837

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6394925A>G , CM000673.2:g.6394925A>G GRCh38
NC_000011.9:g.6416155A>G , CM000673.1:g.6416155A>G GRCh37
NC_000011.8:g.6372731A>G NCBI36
NG_011780.1:g.9501A>G
NG_029615.1:g.29490T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.*318A>G MANE Select ENSP00000340409.4:n.*318A>G
ENST00000342245.8:c.*318A>G ENSP00000340409.4:n.*318A>G
ENST00000526280.1:c.1271A>G
ENST00000533123.5:c.*941A>G ENSP00000435950.1:n.*941A>G
ENST00000534405.5:c.*1045A>G ENSP00000434353.1:n.*1045A>G
NM_000543.4:c.*318A>G NP_000534.3:n.*318A>G
NM_001007593.2:c.*318A>G NP_001007594.2:n.*318A>G
XM_011520303.1:c.*318A>G XP_011518605.1:n.*318A>G
NM_001318087.1:c.*707A>G NP_001305016.1:n.*707A>G
NM_001318088.1:c.*318A>G NP_001305017.1:n.*318A>G
NM_001365135.1:c.*318A>G NP_001352064.1:n.*318A>G
NR_027400.2:n.2227A>G
NR_134502.1:n.1766A>G
XR_001747940.2:n.2399A>G
XR_002957158.1:n.2581A>G
NM_000543.5:c.*318A>G MANE Select NP_000534.3:n.*318A>G
NM_001007593.3:c.*318A>G NP_001007594.2:n.*318A>G
NM_001318087.2:c.*707A>G NP_001305016.1:n.*707A>G
NM_001318088.2:c.*318A>G NP_001305017.1:n.*318A>G
NM_001365135.2:c.*318A>G NP_001352064.1:n.*318A>G
NR_027400.3:n.2167A>G
NR_134502.2:n.1706A>G