Canonical Allele Identifier: CA2740093619

Gene: SMPD1

Linked Data

• ClinVar Variation Id: 2949931
• ClinVar RCV Id: RCV003807289

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394184C>G , CM000673.2:g.6394184C>G	GRCh38
NC_000011.9:g.6415414C>G , CM000673.1:g.6415414C>G	GRCh37
NC_000011.8:g.6371990C>G	NCBI36
NG_011780.1:g.8760C>G
NG_029615.1:g.30231G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1487-14C>G MANE Select	ENSP00000340409.4:n.1487-14C>G
ENST00000342245.8:c.1487-14C>G	ENSP00000340409.4:n.1487-14C>G
ENST00000526280.1:c.544-14C>G
ENST00000527275.5:c.1484-14C>G	ENSP00000435350.1:n.1484-14C>G
ENST00000531303.5:c.*324C>G	ENSP00000432625.1:n.*324C>G
ENST00000531336.1:n.461C>G
ENST00000533123.5:c.*214-14C>G	ENSP00000435950.1:n.*214-14C>G
ENST00000534405.5:c.*318-14C>G	ENSP00000434353.1:n.*318-14C>G
NM_000543.4:c.1487-14C>G	NP_000534.3:n.1487-14C>G
NM_001007593.2:c.1484-14C>G	NP_001007594.2:n.1484-14C>G
XM_005253075.3:c.1493C>G	XP_005253132.1:p.Pro498Arg
XM_011520303.1:c.1355-14C>G	XP_011518605.1:n.1355-14C>G
XM_011520304.1:c.1361C>G	XP_011518606.1:p.Pro454Arg
NM_001318087.1:c.1493C>G	NP_001305016.1:p.Pro498Arg
NM_001318088.1:c.566-14C>G	NP_001305017.1:n.566-14C>G
NM_001365135.1:c.1355-14C>G	NP_001352064.1:n.1355-14C>G
NR_027400.2:n.1500-14C>G
NR_134502.1:n.1025C>G
XM_011520304.2:c.1361C>G	XP_011518606.1:p.Pro454Arg
XR_001747940.2:n.1658C>G
XR_002957158.1:n.1854-14C>G
NM_000543.5:c.1487-14C>G MANE Select	NP_000534.3:n.1487-14C>G
NM_001007593.3:c.1484-14C>G	NP_001007594.2:n.1484-14C>G
NM_001318087.2:c.1493C>G	NP_001305016.1:p.Pro498Arg
NM_001318088.2:c.566-14C>G	NP_001305017.1:n.566-14C>G
NM_001365135.2:c.1355-14C>G	NP_001352064.1:n.1355-14C>G
NR_027400.3:n.1440-14C>G
NR_134502.2:n.965C>G