Canonical Allele Identifier: CA217301969

Gene: SMPD1

Linked Data

• ClinVar Variation Id: 1501508
• ClinVar RCV Id: RCV002017523
• dbSNP Id: rs140688153
• MyVariant Identifiers: chr11:g.6414871C>T (hg19) ; chr11:g.6393641C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393641C>T , CM000673.2:g.6393641C>T	GRCh38
NC_000011.9:g.6414871C>T , CM000673.1:g.6414871C>T	GRCh37
NC_000011.8:g.6371447C>T	NCBI36
NG_011780.1:g.8217C>T
NG_029615.1:g.30774G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1288C>T MANE Select	ENSP00000340409.4:p.Pro430Ser
ENST00000342245.8:c.1288C>T	ENSP00000340409.4:p.Pro430Ser
ENST00000526280.1:c.345C>T
ENST00000527275.5:c.1285C>T	ENSP00000435350.1:p.Pro429Ser
ENST00000531303.5:c.*119C>T	ENSP00000432625.1:n.*119C>T
ENST00000531336.1:n.120C>T
ENST00000532367.1:n.124C>T
ENST00000533123.5:c.*15C>T	ENSP00000435950.1:n.*15C>T
ENST00000534405.5:c.*119C>T	ENSP00000434353.1:n.*119C>T
NM_000543.4:c.1288C>T	NP_000534.3:p.Pro430Ser
NM_001007593.2:c.1285C>T	NP_001007594.2:p.Pro429Ser
XM_005253075.3:c.1288C>T	XP_005253132.1:p.Pro430Ser
XM_011520303.1:c.1156C>T	XP_011518605.1:p.Pro386Ser
XM_011520304.1:c.1156C>T	XP_011518606.1:p.Pro386Ser
XR_930886.1:n.1626C>T
NM_001318087.1:c.1288C>T	NP_001305016.1:p.Pro430Ser
NM_001318088.1:c.367C>T	NP_001305017.1:p.Pro123Ser
NM_001365135.1:c.1156C>T	NP_001352064.1:p.Pro386Ser
NR_027400.2:n.1301C>T
NR_134502.1:n.820C>T
XM_011520304.2:c.1156C>T	XP_011518606.1:p.Pro386Ser
XR_001747940.2:n.1453C>T
XR_002957158.1:n.1453C>T
NM_000543.5:c.1288C>T MANE Select	NP_000534.3:p.Pro430Ser
NM_001007593.3:c.1285C>T	NP_001007594.2:p.Pro429Ser
NM_001318087.2:c.1288C>T	NP_001305016.1:p.Pro430Ser
NM_001318088.2:c.367C>T	NP_001305017.1:p.Pro123Ser
NM_001365135.2:c.1156C>T	NP_001352064.1:p.Pro386Ser
NR_027400.3:n.1241C>T
NR_134502.2:n.760C>T