Canonical Allele Identifier: CA472910023

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415264T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394034T>G , CM000673.2:g.6394034T>G	GRCh38
NC_000011.9:g.6415264T>G , CM000673.1:g.6415264T>G	GRCh37
NC_000011.8:g.6371840T>G	NCBI36
NG_011780.1:g.8610T>G
NG_029615.1:g.30381A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1479T>G MANE Select	ENSP00000340409.4:p.Leu493=
ENST00000342245.8:c.1479T>G	ENSP00000340409.4:p.Leu493=
ENST00000526280.1:c.536T>G
ENST00000527275.5:c.1476T>G	ENSP00000435350.1:p.Leu492=
ENST00000531303.5:c.*310T>G	ENSP00000432625.1:n.*310T>G
ENST00000531336.1:n.311T>G
ENST00000532367.1:n.315T>G
ENST00000533123.5:c.*206T>G	ENSP00000435950.1:n.*206T>G
ENST00000534405.5:c.*310T>G	ENSP00000434353.1:n.*310T>G
NM_000543.4:c.1479T>G	NP_000534.3:p.Leu493=
NM_001007593.2:c.1476T>G	NP_001007594.2:p.Leu492=
XM_005253075.3:c.1479T>G	XP_005253132.1:p.Leu493=
XM_011520303.1:c.1347T>G	XP_011518605.1:p.Leu449=
XM_011520304.1:c.1347T>G	XP_011518606.1:p.Leu449=
NM_001318087.1:c.1479T>G	NP_001305016.1:p.Leu493=
NM_001318088.1:c.558T>G	NP_001305017.1:p.Leu186=
NM_001365135.1:c.1347T>G	NP_001352064.1:p.Leu449=
NR_027400.2:n.1492T>G
NR_134502.1:n.1011T>G
XM_011520304.2:c.1347T>G	XP_011518606.1:p.Leu449=
XR_001747940.2:n.1644T>G
XR_002957158.1:n.1846T>G
NM_000543.5:c.1479T>G MANE Select	NP_000534.3:p.Leu493=
NM_001007593.3:c.1476T>G	NP_001007594.2:p.Leu492=
NM_001318087.2:c.1479T>G	NP_001305016.1:p.Leu493=
NM_001318088.2:c.558T>G	NP_001305017.1:p.Leu186=
NM_001365135.2:c.1347T>G	NP_001352064.1:p.Leu449=
NR_027400.3:n.1432T>G
NR_134502.2:n.951T>G