Canonical Allele Identifier: CA472736784

Gene: SMPD1

Linked Data

• ClinVar Variation Id: 1659296
• ClinVar RCV Id: RCV002178399
• dbSNP Id: rs2134018068
• MyVariant Identifiers: chr11:g.6414611A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393381A>C , CM000673.2:g.6393381A>C	GRCh38
NC_000011.9:g.6414611A>C , CM000673.1:g.6414611A>C	GRCh37
NC_000011.8:g.6371187A>C	NCBI36
NG_011780.1:g.7957A>C
NG_029615.1:g.31034T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1257A>C MANE Select	ENSP00000340409.4:p.Gly419=
ENST00000342245.8:c.1257A>C	ENSP00000340409.4:p.Gly419=
ENST00000526280.1:c.321-236A>C
ENST00000527275.5:c.1254A>C	ENSP00000435350.1:p.Gly418=
ENST00000531303.5:c.*88A>C	ENSP00000432625.1:n.*88A>C
ENST00000531336.1:n.89A>C
ENST00000533123.5:c.1092-236A>C	ENSP00000435950.1:n.1092-236A>C
ENST00000534405.5:c.*88A>C	ENSP00000434353.1:n.*88A>C
NM_000543.4:c.1257A>C	NP_000534.3:p.Gly419=
NM_001007593.2:c.1254A>C	NP_001007594.2:p.Gly418=
XM_005253075.3:c.1257A>C	XP_005253132.1:p.Gly419=
XM_011520303.1:c.1132-236A>C	XP_011518605.1:n.1132-236A>C
XM_011520304.1:c.1132-236A>C	XP_011518606.1:n.1132-236A>C
XR_930886.1:n.1595A>C
NM_001318087.1:c.1257A>C	NP_001305016.1:p.Gly419=
NM_001318088.1:c.336A>C	NP_001305017.1:p.Gly112=
NM_001365135.1:c.1132-236A>C	NP_001352064.1:n.1132-236A>C
NR_027400.2:n.1277-236A>C
NR_134502.1:n.789A>C
XM_011520304.2:c.1132-236A>C	XP_011518606.1:n.1132-236A>C
XR_001747940.2:n.1422A>C
XR_002957158.1:n.1422A>C
NM_000543.5:c.1257A>C MANE Select	NP_000534.3:p.Gly419=
NM_001007593.3:c.1254A>C	NP_001007594.2:p.Gly418=
NM_001318087.2:c.1257A>C	NP_001305016.1:p.Gly419=
NM_001318088.2:c.336A>C	NP_001305017.1:p.Gly112=
NM_001365135.2:c.1132-236A>C	NP_001352064.1:n.1132-236A>C
NR_027400.3:n.1217-236A>C
NR_134502.2:n.729A>C