Canonical Allele Identifier: CA379373086

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6414510T>G (hg19) ; chr11:g.6393280T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393280T>G , CM000673.2:g.6393280T>G	GRCh38
NC_000011.9:g.6414510T>G , CM000673.1:g.6414510T>G	GRCh37
NC_000011.8:g.6371086T>G	NCBI36
NG_011780.1:g.7856T>G
NG_029615.1:g.31135A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1156T>G MANE Select	ENSP00000340409.4:p.Phe386Val
ENST00000342245.8:c.1156T>G	ENSP00000340409.4:p.Phe386Val
ENST00000526280.1:c.321-337T>G
ENST00000527275.5:c.1153T>G	ENSP00000435350.1:p.Phe385Val
ENST00000531303.5:c.503T>G	ENSP00000432625.1:p.Phe168Cys
ENST00000533123.5:c.1092-337T>G	ENSP00000435950.1:n.1092-337T>G
ENST00000534405.5:c.1196T>G	ENSP00000434353.1:p.Phe399Cys
NM_000543.4:c.1156T>G	NP_000534.3:p.Phe386Val
NM_001007593.2:c.1153T>G	NP_001007594.2:p.Phe385Val
XM_005253075.3:c.1156T>G	XP_005253132.1:p.Phe386Val
XM_011520303.1:c.1132-337T>G	XP_011518605.1:n.1132-337T>G
XM_011520304.1:c.1132-337T>G	XP_011518606.1:n.1132-337T>G
XR_930886.1:n.1494T>G
NM_001318087.1:c.1156T>G	NP_001305016.1:p.Phe386Val
NM_001318088.1:c.235T>G	NP_001305017.1:p.Phe79Val
NM_001365135.1:c.1132-337T>G	NP_001352064.1:n.1132-337T>G
NR_027400.2:n.1277-337T>G
NR_134502.1:n.688T>G
XM_011520304.2:c.1132-337T>G	XP_011518606.1:n.1132-337T>G
XR_001747940.2:n.1321T>G
XR_002957158.1:n.1321T>G
NM_000543.5:c.1156T>G MANE Select	NP_000534.3:p.Phe386Val
NM_001007593.3:c.1153T>G	NP_001007594.2:p.Phe385Val
NM_001318087.2:c.1156T>G	NP_001305016.1:p.Phe386Val
NM_001318088.2:c.235T>G	NP_001305017.1:p.Phe79Val
NM_001365135.2:c.1132-337T>G	NP_001352064.1:n.1132-337T>G
NR_027400.3:n.1217-337T>G
NR_134502.2:n.628T>G