Canonical Allele Identifier: CA2574738737

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6394680-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394680C>A , CM000673.2:g.6394680C>A	GRCh38
NC_000011.9:g.6415910C>A , CM000673.1:g.6415910C>A	GRCh37
NC_000011.8:g.6372486C>A	NCBI36
NG_011780.1:g.9256C>A
NG_029615.1:g.29735G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*73C>A MANE Select	ENSP00000340409.4:n.*73C>A
ENST00000342245.8:c.*73C>A	ENSP00000340409.4:n.*73C>A
ENST00000526280.1:c.1026C>A
ENST00000527275.5:c.*73C>A	ENSP00000435350.1:n.*73C>A
ENST00000531303.5:c.*820C>A	ENSP00000432625.1:n.*820C>A
ENST00000533123.5:c.*696C>A	ENSP00000435950.1:n.*696C>A
ENST00000534405.5:c.*800C>A	ENSP00000434353.1:n.*800C>A
NM_000543.4:c.*73C>A	NP_000534.3:n.*73C>A
NM_001007593.2:c.*73C>A	NP_001007594.2:n.*73C>A
XM_011520303.1:c.*73C>A	XP_011518605.1:n.*73C>A
NM_001318087.1:c.*462C>A	NP_001305016.1:n.*462C>A
NM_001318088.1:c.*73C>A	NP_001305017.1:n.*73C>A
NM_001365135.1:c.*73C>A	NP_001352064.1:n.*73C>A
NR_027400.2:n.1982C>A
NR_134502.1:n.1521C>A
XR_001747940.2:n.2154C>A
XR_002957158.1:n.2336C>A
NM_000543.5:c.*73C>A MANE Select	NP_000534.3:n.*73C>A
NM_001007593.3:c.*73C>A	NP_001007594.2:n.*73C>A
NM_001318087.2:c.*462C>A	NP_001305016.1:n.*462C>A
NM_001318088.2:c.*73C>A	NP_001305017.1:n.*73C>A
NM_001365135.2:c.*73C>A	NP_001352064.1:n.*73C>A
NR_027400.3:n.1922C>A
NR_134502.2:n.1461C>A