Canonical Allele Identifier: CA379376343

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415517G>C (hg19) ; chr11:g.6394287G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394287G>C , CM000673.2:g.6394287G>C	GRCh38
NC_000011.9:g.6415517G>C , CM000673.1:g.6415517G>C	GRCh37
NC_000011.8:g.6372093G>C	NCBI36
NG_011780.1:g.8863G>C
NG_029615.1:g.30128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1576G>C MANE Select	ENSP00000340409.4:p.Ala526Pro
ENST00000342245.8:c.1576G>C	ENSP00000340409.4:p.Ala526Pro
ENST00000526280.1:c.633G>C
ENST00000527275.5:c.1573G>C	ENSP00000435350.1:p.Ala525Pro
ENST00000531303.5:c.*427G>C	ENSP00000432625.1:n.*427G>C
ENST00000531336.1:n.564G>C
ENST00000533123.5:c.*303G>C	ENSP00000435950.1:n.*303G>C
ENST00000534405.5:c.*407G>C	ENSP00000434353.1:n.*407G>C
NM_000543.4:c.1576G>C	NP_000534.3:p.Ala526Pro
NM_001007593.2:c.1573G>C	NP_001007594.2:p.Ala525Pro
XM_005253075.3:c.*69G>C	XP_005253132.1:n.*69G>C
XM_011520303.1:c.1444G>C	XP_011518605.1:p.Ala482Pro
XM_011520304.1:c.*69G>C	XP_011518606.1:n.*69G>C
NM_001318087.1:c.*69G>C	NP_001305016.1:n.*69G>C
NM_001318088.1:c.655G>C	NP_001305017.1:p.Ala219Pro
NM_001365135.1:c.1444G>C	NP_001352064.1:p.Ala482Pro
NR_027400.2:n.1589G>C
NR_134502.1:n.1128G>C
XM_011520304.2:c.*69G>C	XP_011518606.1:n.*69G>C
XR_001747940.2:n.1761G>C
XR_002957158.1:n.1943G>C
NM_000543.5:c.1576G>C MANE Select	NP_000534.3:p.Ala526Pro
NM_001007593.3:c.1573G>C	NP_001007594.2:p.Ala525Pro
NM_001318087.2:c.*69G>C	NP_001305016.1:n.*69G>C
NM_001318088.2:c.655G>C	NP_001305017.1:p.Ala219Pro
NM_001365135.2:c.1444G>C	NP_001352064.1:p.Ala482Pro
NR_027400.3:n.1529G>C
NR_134502.2:n.1068G>C