Canonical Allele Identifier: CA5852859

Gene: SMPD1

Linked Data

• ClinVar Variation Id: 2928840
• ClinVar RCV Id: RCV003789614
• dbSNP Id: rs772212665
• ExAC: 11:6414934 G / T
• gnomAD v2: 11-6414934-G-T
• gnomAD v4: 11-6393704-G-T
• MyVariant Identifiers: chr11:g.6414934G>T (hg19) ; chr11:g.6393704G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393704G>T , CM000673.2:g.6393704G>T	GRCh38
NC_000011.9:g.6414934G>T , CM000673.1:g.6414934G>T	GRCh37
NC_000011.8:g.6371510G>T	NCBI36
NG_011780.1:g.8280G>T
NG_029615.1:g.30711C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1340+11G>T MANE Select	ENSP00000340409.4:n.1340+11G>T
ENST00000342245.8:c.1340+11G>T	ENSP00000340409.4:n.1340+11G>T
ENST00000526280.1:c.397+11G>T
ENST00000527275.5:c.1337+11G>T	ENSP00000435350.1:n.1337+11G>T
ENST00000531303.5:c.*171+11G>T	ENSP00000432625.1:n.*171+11G>T
ENST00000531336.1:n.172+11G>T
ENST00000532367.1:n.176+11G>T
ENST00000533123.5:c.*67+11G>T	ENSP00000435950.1:n.*67+11G>T
ENST00000534405.5:c.*171+11G>T	ENSP00000434353.1:n.*171+11G>T
NM_000543.4:c.1340+11G>T	NP_000534.3:n.1340+11G>T
NM_001007593.2:c.1337+11G>T	NP_001007594.2:n.1337+11G>T
XM_005253075.3:c.1340+11G>T	XP_005253132.1:n.1340+11G>T
XM_011520303.1:c.1208+11G>T	XP_011518605.1:n.1208+11G>T
XM_011520304.1:c.1208+11G>T	XP_011518606.1:n.1208+11G>T
XR_930886.1:n.1678+11G>T
NM_001318087.1:c.1340+11G>T	NP_001305016.1:n.1340+11G>T
NM_001318088.1:c.419+11G>T	NP_001305017.1:n.419+11G>T
NM_001365135.1:c.1208+11G>T	NP_001352064.1:n.1208+11G>T
NR_027400.2:n.1353+11G>T
NR_134502.1:n.872+11G>T
XM_011520304.2:c.1208+11G>T	XP_011518606.1:n.1208+11G>T
XR_001747940.2:n.1505+11G>T
XR_002957158.1:n.1516G>T
NM_000543.5:c.1340+11G>T MANE Select	NP_000534.3:n.1340+11G>T
NM_001007593.3:c.1337+11G>T	NP_001007594.2:n.1337+11G>T
NM_001318087.2:c.1340+11G>T	NP_001305016.1:n.1340+11G>T
NM_001318088.2:c.419+11G>T	NP_001305017.1:n.419+11G>T
NM_001365135.2:c.1208+11G>T	NP_001352064.1:n.1208+11G>T
NR_027400.3:n.1293+11G>T
NR_134502.2:n.812+11G>T