Canonical Allele Identifier: CA597438317

Gene: SMPD1

Linked Data

• dbSNP Id: rs1258617179
• gnomAD v2: 11-6414414-A-C
• gnomAD v3: 11-6393184-A-C
• gnomAD v4: 11-6393184-A-C
• MyVariant Identifiers: chr11:g.6414414A>C (hg19) ; chr11:g.6393184A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393184A>C , CM000673.2:g.6393184A>C	GRCh38
NC_000011.9:g.6414414A>C , CM000673.1:g.6414414A>C	GRCh37
NC_000011.8:g.6370990A>C	NCBI36
NG_011780.1:g.7760A>C
NG_029615.1:g.31231T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1092-32A>C MANE Select	ENSP00000340409.4:n.1092-32A>C
ENST00000342245.8:c.1092-32A>C	ENSP00000340409.4:n.1092-32A>C
ENST00000526280.1:c.321-433A>C
ENST00000527275.5:c.1089-32A>C	ENSP00000435350.1:n.1089-32A>C
ENST00000531303.5:c.439-32A>C	ENSP00000432625.1:n.439-32A>C
ENST00000533123.5:c.1092-433A>C	ENSP00000435950.1:n.1092-433A>C
ENST00000534405.5:c.1132-32A>C	ENSP00000434353.1:n.1132-32A>C
NM_000543.4:c.1092-32A>C	NP_000534.3:n.1092-32A>C
NM_001007593.2:c.1089-32A>C	NP_001007594.2:n.1089-32A>C
XM_005253075.3:c.1092-32A>C	XP_005253132.1:n.1092-32A>C
XM_011520303.1:c.1132-433A>C	XP_011518605.1:n.1132-433A>C
XM_011520304.1:c.1132-433A>C	XP_011518606.1:n.1132-433A>C
XR_930886.1:n.1430-32A>C
NM_001318087.1:c.1092-32A>C	NP_001305016.1:n.1092-32A>C
NM_001318088.1:c.171-32A>C	NP_001305017.1:n.171-32A>C
NM_001365135.1:c.1132-433A>C	NP_001352064.1:n.1132-433A>C
NR_027400.2:n.1277-433A>C
NR_134502.1:n.624-32A>C
XM_011520304.2:c.1132-433A>C	XP_011518606.1:n.1132-433A>C
XR_001747940.2:n.1257-32A>C
XR_002957158.1:n.1257-32A>C
NM_000543.5:c.1092-32A>C MANE Select	NP_000534.3:n.1092-32A>C
NM_001007593.3:c.1089-32A>C	NP_001007594.2:n.1089-32A>C
NM_001318087.2:c.1092-32A>C	NP_001305016.1:n.1092-32A>C
NM_001318088.2:c.171-32A>C	NP_001305017.1:n.171-32A>C
NM_001365135.2:c.1132-433A>C	NP_001352064.1:n.1132-433A>C
NR_027400.3:n.1217-433A>C
NR_134502.2:n.564-32A>C