Canonical Allele Identifier: CA472736698

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6414524G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393294G>A , CM000673.2:g.6393294G>A	GRCh38
NC_000011.9:g.6414524G>A , CM000673.1:g.6414524G>A	GRCh37
NC_000011.8:g.6371100G>A	NCBI36
NG_011780.1:g.7870G>A
NG_029615.1:g.31121C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1170G>A MANE Select	ENSP00000340409.4:p.Glu390=
ENST00000342245.8:c.1170G>A	ENSP00000340409.4:p.Glu390=
ENST00000526280.1:c.321-323G>A
ENST00000527275.5:c.1167G>A	ENSP00000435350.1:p.Glu389=
ENST00000531303.5:c.*1G>A	ENSP00000432625.1:n.*1G>A
ENST00000531336.1:n.2G>A
ENST00000533123.5:c.1092-323G>A	ENSP00000435950.1:n.1092-323G>A
ENST00000534405.5:c.*1G>A	ENSP00000434353.1:n.*1G>A
NM_000543.4:c.1170G>A	NP_000534.3:p.Glu390=
NM_001007593.2:c.1167G>A	NP_001007594.2:p.Glu389=
XM_005253075.3:c.1170G>A	XP_005253132.1:p.Glu390=
XM_011520303.1:c.1132-323G>A	XP_011518605.1:n.1132-323G>A
XM_011520304.1:c.1132-323G>A	XP_011518606.1:n.1132-323G>A
XR_930886.1:n.1508G>A
NM_001318087.1:c.1170G>A	NP_001305016.1:p.Glu390=
NM_001318088.1:c.249G>A	NP_001305017.1:p.Glu83=
NM_001365135.1:c.1132-323G>A	NP_001352064.1:n.1132-323G>A
NR_027400.2:n.1277-323G>A
NR_134502.1:n.702G>A
XM_011520304.2:c.1132-323G>A	XP_011518606.1:n.1132-323G>A
XR_001747940.2:n.1335G>A
XR_002957158.1:n.1335G>A
NM_000543.5:c.1170G>A MANE Select	NP_000534.3:p.Glu390=
NM_001007593.3:c.1167G>A	NP_001007594.2:p.Glu389=
NM_001318087.2:c.1170G>A	NP_001305016.1:p.Glu390=
NM_001318088.2:c.249G>A	NP_001305017.1:p.Glu83=
NM_001365135.2:c.1132-323G>A	NP_001352064.1:n.1132-323G>A
NR_027400.3:n.1217-323G>A
NR_134502.2:n.642G>A