Canonical Allele Identifier: CA472909478

Gene: SMPD1

Linked Data

• ClinVar Variation Id: 1745798
• ClinVar RCV Id: RCV002338390 ; RCV003102697
• dbSNP Id: rs1472925913
• gnomAD v2: 11-6412811-T-C
• gnomAD v3: 11-6391581-T-C
• gnomAD v4: 11-6391581-T-C
• MyVariant Identifiers: chr11:g.6412811T>C (hg19) ; chr11:g.6391581T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391581T>C , CM000673.2:g.6391581T>C	GRCh38
NC_000011.9:g.6412811T>C , CM000673.1:g.6412811T>C	GRCh37
NC_000011.8:g.6369387T>C	NCBI36
NG_011780.1:g.6157T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.516T>C MANE Select	ENSP00000340409.4:p.Ile172=
ENST00000342245.8:c.516T>C	ENSP00000340409.4:p.Ile172=
ENST00000527275.5:c.513T>C	ENSP00000435350.1:p.Ile171=
ENST00000530395.1:c.-95-209T>C	ENSP00000431479.1:n.-95-209T>C
ENST00000531303.5:c.438+78T>C	ENSP00000432625.1:n.438+78T>C
ENST00000533123.5:c.516T>C	ENSP00000435950.1:p.Ile172=
ENST00000533196.1:n.375-425T>C
ENST00000534405.5:c.516T>C	ENSP00000434353.1:p.Ile172=
NM_000543.4:c.516T>C	NP_000534.3:p.Ile172=
NM_001007593.2:c.513T>C	NP_001007594.2:p.Ile171=
XM_005253075.3:c.516T>C	XP_005253132.1:p.Ile172=
XM_011520303.1:c.516T>C	XP_011518605.1:p.Ile172=
XM_011520304.1:c.516T>C	XP_011518606.1:p.Ile172=
XR_930886.1:n.814T>C
NM_001318087.1:c.516T>C	NP_001305016.1:p.Ile172=
NM_001318088.1:c.-446T>C	NP_001305017.1:n.-446T>C
NM_001365135.1:c.516T>C	NP_001352064.1:p.Ile172=
NR_027400.2:n.701T>C
NR_134502.1:n.623+78T>C
XM_011520304.2:c.516T>C	XP_011518606.1:p.Ile172=
XR_001747940.2:n.641T>C
XR_002957158.1:n.641T>C
NM_000543.5:c.516T>C MANE Select	NP_000534.3:p.Ile172=
NM_001007593.3:c.513T>C	NP_001007594.2:p.Ile171=
NM_001318087.2:c.516T>C	NP_001305016.1:p.Ile172=
NM_001318088.2:c.-446T>C	NP_001305017.1:n.-446T>C
NM_001365135.2:c.516T>C	NP_001352064.1:p.Ile172=
NR_027400.3:n.641T>C
NR_134502.2:n.563+78T>C