Canonical Allele Identifier: CA379376154

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6415490G>A (hg19) ; chr11:g.6394260G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394260G>A , CM000673.2:g.6394260G>A	GRCh38
NC_000011.9:g.6415490G>A , CM000673.1:g.6415490G>A	GRCh37
NC_000011.8:g.6372066G>A	NCBI36
NG_011780.1:g.8836G>A
NG_029615.1:g.30155C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1549G>A MANE Select	ENSP00000340409.4:p.Glu517Lys
ENST00000342245.8:c.1549G>A	ENSP00000340409.4:p.Glu517Lys
ENST00000526280.1:c.606G>A
ENST00000527275.5:c.1546G>A	ENSP00000435350.1:p.Glu516Lys
ENST00000531303.5:c.*400G>A	ENSP00000432625.1:n.*400G>A
ENST00000531336.1:n.537G>A
ENST00000533123.5:c.*276G>A	ENSP00000435950.1:n.*276G>A
ENST00000534405.5:c.*380G>A	ENSP00000434353.1:n.*380G>A
NM_000543.4:c.1549G>A	NP_000534.3:p.Glu517Lys
NM_001007593.2:c.1546G>A	NP_001007594.2:p.Glu516Lys
XM_005253075.3:c.*42G>A	XP_005253132.1:n.*42G>A
XM_011520303.1:c.1417G>A	XP_011518605.1:p.Glu473Lys
XM_011520304.1:c.*42G>A	XP_011518606.1:n.*42G>A
NM_001318087.1:c.*42G>A	NP_001305016.1:n.*42G>A
NM_001318088.1:c.628G>A	NP_001305017.1:p.Glu210Lys
NM_001365135.1:c.1417G>A	NP_001352064.1:p.Glu473Lys
NR_027400.2:n.1562G>A
NR_134502.1:n.1101G>A
XM_011520304.2:c.*42G>A	XP_011518606.1:n.*42G>A
XR_001747940.2:n.1734G>A
XR_002957158.1:n.1916G>A
NM_000543.5:c.1549G>A MANE Select	NP_000534.3:p.Glu517Lys
NM_001007593.3:c.1546G>A	NP_001007594.2:p.Glu516Lys
NM_001318087.2:c.*42G>A	NP_001305016.1:n.*42G>A
NM_001318088.2:c.628G>A	NP_001305017.1:p.Glu210Lys
NM_001365135.2:c.1417G>A	NP_001352064.1:p.Glu473Lys
NR_027400.3:n.1502G>A
NR_134502.2:n.1041G>A