Canonical Allele Identifier: CA379376414

Gene: SMPD1

Linked Data

• dbSNP Id: rs772417462
• MyVariant Identifiers: chr11:g.6415527C>G (hg19) ; chr11:g.6394297C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394297C>G , CM000673.2:g.6394297C>G	GRCh38
NC_000011.9:g.6415527C>G , CM000673.1:g.6415527C>G	GRCh37
NC_000011.8:g.6372103C>G	NCBI36
NG_011780.1:g.8873C>G
NG_029615.1:g.30118G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1586C>G MANE Select	ENSP00000340409.4:p.Pro529Arg
ENST00000342245.8:c.1586C>G	ENSP00000340409.4:p.Pro529Arg
ENST00000526280.1:c.643C>G
ENST00000527275.5:c.1583C>G	ENSP00000435350.1:p.Pro528Arg
ENST00000531303.5:c.*437C>G	ENSP00000432625.1:n.*437C>G
ENST00000531336.1:n.574C>G
ENST00000533123.5:c.*313C>G	ENSP00000435950.1:n.*313C>G
ENST00000534405.5:c.*417C>G	ENSP00000434353.1:n.*417C>G
NM_000543.4:c.1586C>G	NP_000534.3:p.Pro529Arg
NM_001007593.2:c.1583C>G	NP_001007594.2:p.Pro528Arg
XM_005253075.3:c.*79C>G	XP_005253132.1:n.*79C>G
XM_011520303.1:c.1454C>G	XP_011518605.1:p.Pro485Arg
XM_011520304.1:c.*79C>G	XP_011518606.1:n.*79C>G
NM_001318087.1:c.*79C>G	NP_001305016.1:n.*79C>G
NM_001318088.1:c.665C>G	NP_001305017.1:p.Pro222Arg
NM_001365135.1:c.1454C>G	NP_001352064.1:p.Pro485Arg
NR_027400.2:n.1599C>G
NR_134502.1:n.1138C>G
XM_011520304.2:c.*79C>G	XP_011518606.1:n.*79C>G
XR_001747940.2:n.1771C>G
XR_002957158.1:n.1953C>G
NM_000543.5:c.1586C>G MANE Select	NP_000534.3:p.Pro529Arg
NM_001007593.3:c.1583C>G	NP_001007594.2:p.Pro528Arg
NM_001318087.2:c.*79C>G	NP_001305016.1:n.*79C>G
NM_001318088.2:c.665C>G	NP_001305017.1:p.Pro222Arg
NM_001365135.2:c.1454C>G	NP_001352064.1:p.Pro485Arg
NR_027400.3:n.1539C>G
NR_134502.2:n.1078C>G