Canonical Allele Identifier: CA379369771

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6412812T>G (hg19) ; chr11:g.6391582T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391582T>G , CM000673.2:g.6391582T>G	GRCh38
NC_000011.9:g.6412812T>G , CM000673.1:g.6412812T>G	GRCh37
NC_000011.8:g.6369388T>G	NCBI36
NG_011780.1:g.6158T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.517T>G MANE Select	ENSP00000340409.4:p.Phe173Val
ENST00000342245.8:c.517T>G	ENSP00000340409.4:p.Phe173Val
ENST00000527275.5:c.514T>G	ENSP00000435350.1:p.Phe172Val
ENST00000530395.1:c.-95-208T>G	ENSP00000431479.1:n.-95-208T>G
ENST00000531303.5:c.438+79T>G	ENSP00000432625.1:n.438+79T>G
ENST00000533123.5:c.517T>G	ENSP00000435950.1:p.Phe173Val
ENST00000533196.1:n.375-424T>G
ENST00000534405.5:c.517T>G	ENSP00000434353.1:p.Phe173Val
NM_000543.4:c.517T>G	NP_000534.3:p.Phe173Val
NM_001007593.2:c.514T>G	NP_001007594.2:p.Phe172Val
XM_005253075.3:c.517T>G	XP_005253132.1:p.Phe173Val
XM_011520303.1:c.517T>G	XP_011518605.1:p.Phe173Val
XM_011520304.1:c.517T>G	XP_011518606.1:p.Phe173Val
XR_930886.1:n.815T>G
NM_001318087.1:c.517T>G	NP_001305016.1:p.Phe173Val
NM_001318088.1:c.-445T>G	NP_001305017.1:n.-445T>G
NM_001365135.1:c.517T>G	NP_001352064.1:p.Phe173Val
NR_027400.2:n.702T>G
NR_134502.1:n.623+79T>G
XM_011520304.2:c.517T>G	XP_011518606.1:p.Phe173Val
XR_001747940.2:n.642T>G
XR_002957158.1:n.642T>G
NM_000543.5:c.517T>G MANE Select	NP_000534.3:p.Phe173Val
NM_001007593.3:c.514T>G	NP_001007594.2:p.Phe172Val
NM_001318087.2:c.517T>G	NP_001305016.1:p.Phe173Val
NM_001318088.2:c.-445T>G	NP_001305017.1:n.-445T>G
NM_001365135.2:c.517T>G	NP_001352064.1:p.Phe173Val
NR_027400.3:n.642T>G
NR_134502.2:n.563+79T>G