Canonical Allele Identifier: CA379371273

Gene: SMPD1

Linked Data

• MyVariant Identifiers: chr11:g.6413212G>T (hg19) ; chr11:g.6391982G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391982G>T , CM000673.2:g.6391982G>T	GRCh38
NC_000011.9:g.6413212G>T , CM000673.1:g.6413212G>T	GRCh37
NC_000011.8:g.6369788G>T	NCBI36
NG_011780.1:g.6558G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.917G>T MANE Select	ENSP00000340409.4:p.Arg306Met
ENST00000342245.8:c.917G>T	ENSP00000340409.4:p.Arg306Met
ENST00000526280.1:c.106G>T
ENST00000527275.5:c.914G>T	ENSP00000435350.1:p.Arg305Met
ENST00000530395.1:c.98G>T	ENSP00000431479.1:p.Arg33Met
ENST00000531303.5:c.438+479G>T	ENSP00000432625.1:n.438+479G>T
ENST00000533123.5:c.917G>T	ENSP00000435950.1:p.Arg306Met
ENST00000533196.1:n.375-24G>T
ENST00000534405.5:c.917G>T	ENSP00000434353.1:p.Arg306Met
NM_000543.4:c.917G>T	NP_000534.3:p.Arg306Met
NM_001007593.2:c.914G>T	NP_001007594.2:p.Arg305Met
XM_005253075.3:c.917G>T	XP_005253132.1:p.Arg306Met
XM_011520303.1:c.917G>T	XP_011518605.1:p.Arg306Met
XM_011520304.1:c.917G>T	XP_011518606.1:p.Arg306Met
XR_930886.1:n.1215G>T
NM_001318087.1:c.917G>T	NP_001305016.1:p.Arg306Met
NM_001318088.1:c.-45G>T	NP_001305017.1:n.-45G>T
NM_001365135.1:c.917G>T	NP_001352064.1:p.Arg306Met
NR_027400.2:n.1102G>T
NR_134502.1:n.623+479G>T
XM_011520304.2:c.917G>T	XP_011518606.1:p.Arg306Met
XR_001747940.2:n.1042G>T
XR_002957158.1:n.1042G>T
NM_000543.5:c.917G>T MANE Select	NP_000534.3:p.Arg306Met
NM_001007593.3:c.914G>T	NP_001007594.2:p.Arg305Met
NM_001318087.2:c.917G>T	NP_001305016.1:p.Arg306Met
NM_001318088.2:c.-45G>T	NP_001305017.1:n.-45G>T
NM_001365135.2:c.917G>T	NP_001352064.1:p.Arg306Met
NR_027400.3:n.1042G>T
NR_134502.2:n.563+479G>T