Canonical Allele Identifier: CA379373003

Gene: SMPD1

Linked Data

• ClinVar Variation Id: 2103537
• ClinVar RCV Id: RCV003022199
• MyVariant Identifiers: chr11:g.6414498C>G (hg19) ; chr11:g.6393268C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393268C>G , CM000673.2:g.6393268C>G	GRCh38
NC_000011.9:g.6414498C>G , CM000673.1:g.6414498C>G	GRCh37
NC_000011.8:g.6371074C>G	NCBI36
NG_011780.1:g.7844C>G
NG_029615.1:g.31147G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1144C>G MANE Select	ENSP00000340409.4:p.Leu382Val
ENST00000342245.8:c.1144C>G	ENSP00000340409.4:p.Leu382Val
ENST00000526280.1:c.321-349C>G
ENST00000527275.5:c.1141C>G	ENSP00000435350.1:p.Leu381Val
ENST00000531303.5:c.491C>G	ENSP00000432625.1:p.Ser164Cys
ENST00000533123.5:c.1092-349C>G	ENSP00000435950.1:n.1092-349C>G
ENST00000534405.5:c.1184C>G	ENSP00000434353.1:p.Ser395Cys
NM_000543.4:c.1144C>G	NP_000534.3:p.Leu382Val
NM_001007593.2:c.1141C>G	NP_001007594.2:p.Leu381Val
XM_005253075.3:c.1144C>G	XP_005253132.1:p.Leu382Val
XM_011520303.1:c.1132-349C>G	XP_011518605.1:n.1132-349C>G
XM_011520304.1:c.1132-349C>G	XP_011518606.1:n.1132-349C>G
XR_930886.1:n.1482C>G
NM_001318087.1:c.1144C>G	NP_001305016.1:p.Leu382Val
NM_001318088.1:c.223C>G	NP_001305017.1:p.Leu75Val
NM_001365135.1:c.1132-349C>G	NP_001352064.1:n.1132-349C>G
NR_027400.2:n.1277-349C>G
NR_134502.1:n.676C>G
XM_011520304.2:c.1132-349C>G	XP_011518606.1:n.1132-349C>G
XR_001747940.2:n.1309C>G
XR_002957158.1:n.1309C>G
NM_000543.5:c.1144C>G MANE Select	NP_000534.3:p.Leu382Val
NM_001007593.3:c.1141C>G	NP_001007594.2:p.Leu381Val
NM_001318087.2:c.1144C>G	NP_001305016.1:p.Leu382Val
NM_001318088.2:c.223C>G	NP_001305017.1:p.Leu75Val
NM_001365135.2:c.1132-349C>G	NP_001352064.1:n.1132-349C>G
NR_027400.3:n.1217-349C>G
NR_134502.2:n.616C>G