Canonical Allele Identifier: CA2612224149

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6394639-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394639G>A , CM000673.2:g.6394639G>A	GRCh38
NC_000011.9:g.6415869G>A , CM000673.1:g.6415869G>A	GRCh37
NC_000011.8:g.6372445G>A	NCBI36
NG_011780.1:g.9215G>A
NG_029615.1:g.29776C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*32G>A MANE Select	ENSP00000340409.4:n.*32G>A
ENST00000342245.8:c.*32G>A	ENSP00000340409.4:n.*32G>A
ENST00000526280.1:c.985G>A
ENST00000527275.5:c.*32G>A	ENSP00000435350.1:n.*32G>A
ENST00000531303.5:c.*779G>A	ENSP00000432625.1:n.*779G>A
ENST00000533123.5:c.*655G>A	ENSP00000435950.1:n.*655G>A
ENST00000534405.5:c.*759G>A	ENSP00000434353.1:n.*759G>A
NM_000543.4:c.*32G>A	NP_000534.3:n.*32G>A
NM_001007593.2:c.*32G>A	NP_001007594.2:n.*32G>A
XM_011520303.1:c.*32G>A	XP_011518605.1:n.*32G>A
NM_001318087.1:c.*421G>A	NP_001305016.1:n.*421G>A
NM_001318088.1:c.*32G>A	NP_001305017.1:n.*32G>A
NM_001365135.1:c.*32G>A	NP_001352064.1:n.*32G>A
NR_027400.2:n.1941G>A
NR_134502.1:n.1480G>A
XR_001747940.2:n.2113G>A
XR_002957158.1:n.2295G>A
NM_000543.5:c.*32G>A MANE Select	NP_000534.3:n.*32G>A
NM_001007593.3:c.*32G>A	NP_001007594.2:n.*32G>A
NM_001318087.2:c.*421G>A	NP_001305016.1:n.*421G>A
NM_001318088.2:c.*32G>A	NP_001305017.1:n.*32G>A
NM_001365135.2:c.*32G>A	NP_001352064.1:n.*32G>A
NR_027400.3:n.1881G>A
NR_134502.2:n.1420G>A