Canonical Allele Identifier: CA217299659

Gene: SMPD1

Linked Data

• ClinVar Variation Id: 595089
• ClinVar RCV Id: RCV000730536
• dbSNP Id: rs941413871
• gnomAD v4: 11-6391999-G-A
• MyVariant Identifiers: chr11:g.6413229G>A (hg19) ; chr11:g.6391999G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391999G>A , CM000673.2:g.6391999G>A	GRCh38
NC_000011.9:g.6413229G>A , CM000673.1:g.6413229G>A	GRCh37
NC_000011.8:g.6369805G>A	NCBI36
NG_011780.1:g.6575G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.934G>A MANE Select	ENSP00000340409.4:p.Val312Met
ENST00000342245.8:c.934G>A	ENSP00000340409.4:p.Val312Met
ENST00000526280.1:c.123G>A
ENST00000527275.5:c.931G>A	ENSP00000435350.1:p.Val311Met
ENST00000530395.1:c.115G>A	ENSP00000431479.1:p.Val39Met
ENST00000531303.5:c.438+496G>A	ENSP00000432625.1:n.438+496G>A
ENST00000533123.5:c.934G>A	ENSP00000435950.1:p.Val312Met
ENST00000533196.1:n.375-7G>A
ENST00000534405.5:c.934G>A	ENSP00000434353.1:p.Val312Met
NM_000543.4:c.934G>A	NP_000534.3:p.Val312Met
NM_001007593.2:c.931G>A	NP_001007594.2:p.Val311Met
XM_005253075.3:c.934G>A	XP_005253132.1:p.Val312Met
XM_011520303.1:c.934G>A	XP_011518605.1:p.Val312Met
XM_011520304.1:c.934G>A	XP_011518606.1:p.Val312Met
XR_930886.1:n.1232G>A
NM_001318087.1:c.934G>A	NP_001305016.1:p.Val312Met
NM_001318088.1:c.-28G>A	NP_001305017.1:n.-28G>A
NM_001365135.1:c.934G>A	NP_001352064.1:p.Val312Met
NR_027400.2:n.1119G>A
NR_134502.1:n.623+496G>A
XM_011520304.2:c.934G>A	XP_011518606.1:p.Val312Met
XR_001747940.2:n.1059G>A
XR_002957158.1:n.1059G>A
NM_000543.5:c.934G>A MANE Select	NP_000534.3:p.Val312Met
NM_001007593.3:c.931G>A	NP_001007594.2:p.Val311Met
NM_001318087.2:c.934G>A	NP_001305016.1:p.Val312Met
NM_001318088.2:c.-28G>A	NP_001305017.1:n.-28G>A
NM_001365135.2:c.934G>A	NP_001352064.1:p.Val312Met
NR_027400.3:n.1059G>A
NR_134502.2:n.563+496G>A