Canonical Allele Identifier: CA597264389

Gene: SMPD1

Linked Data

• dbSNP Id: rs1383092791
• gnomAD v2: 11-6415917-G-A
• gnomAD v3: 11-6394687-G-A
• gnomAD v4: 11-6394687-G-A
• MyVariant Identifiers: chr11:g.6415917G>A (hg19) ; chr11:g.6394687G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394687G>A , CM000673.2:g.6394687G>A	GRCh38
NC_000011.9:g.6415917G>A , CM000673.1:g.6415917G>A	GRCh37
NC_000011.8:g.6372493G>A	NCBI36
NG_011780.1:g.9263G>A
NG_029615.1:g.29728C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*80G>A MANE Select	ENSP00000340409.4:n.*80G>A
ENST00000342245.8:c.*80G>A	ENSP00000340409.4:n.*80G>A
ENST00000526280.1:c.1033G>A
ENST00000527275.5:c.*80G>A	ENSP00000435350.1:n.*80G>A
ENST00000531303.5:c.*827G>A	ENSP00000432625.1:n.*827G>A
ENST00000533123.5:c.*703G>A	ENSP00000435950.1:n.*703G>A
ENST00000534405.5:c.*807G>A	ENSP00000434353.1:n.*807G>A
NM_000543.4:c.*80G>A	NP_000534.3:n.*80G>A
NM_001007593.2:c.*80G>A	NP_001007594.2:n.*80G>A
XM_011520303.1:c.*80G>A	XP_011518605.1:n.*80G>A
NM_001318087.1:c.*469G>A	NP_001305016.1:n.*469G>A
NM_001318088.1:c.*80G>A	NP_001305017.1:n.*80G>A
NM_001365135.1:c.*80G>A	NP_001352064.1:n.*80G>A
NR_027400.2:n.1989G>A
NR_134502.1:n.1528G>A
XR_001747940.2:n.2161G>A
XR_002957158.1:n.2343G>A
NM_000543.5:c.*80G>A MANE Select	NP_000534.3:n.*80G>A
NM_001007593.3:c.*80G>A	NP_001007594.2:n.*80G>A
NM_001318087.2:c.*469G>A	NP_001305016.1:n.*469G>A
NM_001318088.2:c.*80G>A	NP_001305017.1:n.*80G>A
NM_001365135.2:c.*80G>A	NP_001352064.1:n.*80G>A
NR_027400.3:n.1929G>A
NR_134502.2:n.1468G>A