Canonical Allele Identifier: CA379369832

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6391596-C-A
• MyVariant Identifiers: chr11:g.6412826C>A (hg19) ; chr11:g.6391596C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391596C>A , CM000673.2:g.6391596C>A	GRCh38
NC_000011.9:g.6412826C>A , CM000673.1:g.6412826C>A	GRCh37
NC_000011.8:g.6369402C>A	NCBI36
NG_011780.1:g.6172C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.531C>A MANE Select	ENSP00000340409.4:p.Asn177Lys
ENST00000342245.8:c.531C>A	ENSP00000340409.4:p.Asn177Lys
ENST00000527275.5:c.528C>A	ENSP00000435350.1:p.Asn176Lys
ENST00000530395.1:c.-95-194C>A	ENSP00000431479.1:n.-95-194C>A
ENST00000531303.5:c.438+93C>A	ENSP00000432625.1:n.438+93C>A
ENST00000533123.5:c.531C>A	ENSP00000435950.1:p.Asn177Lys
ENST00000533196.1:n.375-410C>A
ENST00000534405.5:c.531C>A	ENSP00000434353.1:p.Asn177Lys
NM_000543.4:c.531C>A	NP_000534.3:p.Asn177Lys
NM_001007593.2:c.528C>A	NP_001007594.2:p.Asn176Lys
XM_005253075.3:c.531C>A	XP_005253132.1:p.Asn177Lys
XM_011520303.1:c.531C>A	XP_011518605.1:p.Asn177Lys
XM_011520304.1:c.531C>A	XP_011518606.1:p.Asn177Lys
XR_930886.1:n.829C>A
NM_001318087.1:c.531C>A	NP_001305016.1:p.Asn177Lys
NM_001318088.1:c.-431C>A	NP_001305017.1:n.-431C>A
NM_001365135.1:c.531C>A	NP_001352064.1:p.Asn177Lys
NR_027400.2:n.716C>A
NR_134502.1:n.623+93C>A
XM_011520304.2:c.531C>A	XP_011518606.1:p.Asn177Lys
XR_001747940.2:n.656C>A
XR_002957158.1:n.656C>A
NM_000543.5:c.531C>A MANE Select	NP_000534.3:p.Asn177Lys
NM_001007593.3:c.528C>A	NP_001007594.2:p.Asn176Lys
NM_001318087.2:c.531C>A	NP_001305016.1:p.Asn177Lys
NM_001318088.2:c.-431C>A	NP_001305017.1:n.-431C>A
NM_001365135.2:c.531C>A	NP_001352064.1:p.Asn177Lys
NR_027400.3:n.656C>A
NR_134502.2:n.563+93C>A