Canonical Allele Identifier: CA379371575

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413293T>G (hg19) ; chr11:g.6392063T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392063T>G , CM000673.2:g.6392063T>G	GRCh38
NC_000011.9:g.6413293T>G , CM000673.1:g.6413293T>G	GRCh37
NC_000011.8:g.6369869T>G	NCBI36
NG_011780.1:g.6639T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.998T>G MANE Select	ENSP00000340409.4:p.Phe333Cys
ENST00000342245.8:c.998T>G	ENSP00000340409.4:p.Phe333Cys
ENST00000526280.1:c.187T>G
ENST00000527275.5:c.995T>G	ENSP00000435350.1:p.Phe332Cys
ENST00000531303.5:c.438+560T>G	ENSP00000432625.1:n.438+560T>G
ENST00000533123.5:c.998T>G	ENSP00000435950.1:p.Phe333Cys
ENST00000534405.5:c.998T>G	ENSP00000434353.1:p.Phe333Cys
NM_000543.4:c.998T>G	NP_000534.3:p.Phe333Cys
NM_001007593.2:c.995T>G	NP_001007594.2:p.Phe332Cys
XM_005253075.3:c.998T>G	XP_005253132.1:p.Phe333Cys
XM_011520303.1:c.998T>G	XP_011518605.1:p.Phe333Cys
XM_011520304.1:c.998T>G	XP_011518606.1:p.Phe333Cys
XR_930886.1:n.1296T>G
NM_001318087.1:c.998T>G	NP_001305016.1:p.Phe333Cys
NM_001318088.1:c.37T>G	NP_001305017.1:p.Ser13Ala
NM_001365135.1:c.998T>G	NP_001352064.1:p.Phe333Cys
NR_027400.2:n.1183T>G
NR_134502.1:n.623+560T>G
XM_011520304.2:c.998T>G	XP_011518606.1:p.Phe333Cys
XR_001747940.2:n.1123T>G
XR_002957158.1:n.1123T>G
NM_000543.5:c.998T>G MANE Select	NP_000534.3:p.Phe333Cys
NM_001007593.3:c.995T>G	NP_001007594.2:p.Phe332Cys
NM_001318087.2:c.998T>G	NP_001305016.1:p.Phe333Cys
NM_001318088.2:c.37T>G	NP_001305017.1:p.Ser13Ala
NM_001365135.2:c.998T>G	NP_001352064.1:p.Phe333Cys
NR_027400.3:n.1123T>G
NR_134502.2:n.563+560T>G