Canonical Allele Identifier: CA597438316

Gene: SMPD1

Linked Data

• dbSNP Id: rs1225006965
• gnomAD v2: 11-6414409-G-A
• gnomAD v4: 11-6393179-G-A
• MyVariant Identifiers: chr11:g.6414409G>A (hg19) ; chr11:g.6393179G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393179G>A , CM000673.2:g.6393179G>A	GRCh38
NC_000011.9:g.6414409G>A , CM000673.1:g.6414409G>A	GRCh37
NC_000011.8:g.6370985G>A	NCBI36
NG_011780.1:g.7755G>A
NG_029615.1:g.31236C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1092-37G>A MANE Select	ENSP00000340409.4:n.1092-37G>A
ENST00000342245.8:c.1092-37G>A	ENSP00000340409.4:n.1092-37G>A
ENST00000526280.1:c.321-438G>A
ENST00000527275.5:c.1089-37G>A	ENSP00000435350.1:n.1089-37G>A
ENST00000531303.5:c.439-37G>A	ENSP00000432625.1:n.439-37G>A
ENST00000533123.5:c.1092-438G>A	ENSP00000435950.1:n.1092-438G>A
ENST00000534405.5:c.1132-37G>A	ENSP00000434353.1:n.1132-37G>A
NM_000543.4:c.1092-37G>A	NP_000534.3:n.1092-37G>A
NM_001007593.2:c.1089-37G>A	NP_001007594.2:n.1089-37G>A
XM_005253075.3:c.1092-37G>A	XP_005253132.1:n.1092-37G>A
XM_011520303.1:c.1132-438G>A	XP_011518605.1:n.1132-438G>A
XM_011520304.1:c.1132-438G>A	XP_011518606.1:n.1132-438G>A
XR_930886.1:n.1430-37G>A
NM_001318087.1:c.1092-37G>A	NP_001305016.1:n.1092-37G>A
NM_001318088.1:c.171-37G>A	NP_001305017.1:n.171-37G>A
NM_001365135.1:c.1132-438G>A	NP_001352064.1:n.1132-438G>A
NR_027400.2:n.1277-438G>A
NR_134502.1:n.624-37G>A
XM_011520304.2:c.1132-438G>A	XP_011518606.1:n.1132-438G>A
XR_001747940.2:n.1257-37G>A
XR_002957158.1:n.1257-37G>A
NM_000543.5:c.1092-37G>A MANE Select	NP_000534.3:n.1092-37G>A
NM_001007593.3:c.1089-37G>A	NP_001007594.2:n.1089-37G>A
NM_001318087.2:c.1092-37G>A	NP_001305016.1:n.1092-37G>A
NM_001318088.2:c.171-37G>A	NP_001305017.1:n.171-37G>A
NM_001365135.2:c.1132-438G>A	NP_001352064.1:n.1132-438G>A
NR_027400.3:n.1217-438G>A
NR_134502.2:n.564-37G>A