Canonical Allele Identifier: CA1950146416

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391958T= , CM000673.2:g.6391958T=	GRCh38
NC_000011.9:g.6413188T= , CM000673.1:g.6413188T=	GRCh37
NC_000011.8:g.6369764T=	NCBI36
NG_011780.1:g.6534T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.893T= MANE Select	ENSP00000340409.4:p.Leu298=
ENST00000342245.8:c.893T=	ENSP00000340409.4:p.Leu298=
ENST00000526280.1:c.82T=
ENST00000527275.5:c.890T=	ENSP00000435350.1:p.Leu297=
ENST00000530395.1:c.74T=	ENSP00000431479.1:p.Leu25=
ENST00000531303.5:c.438+455T=	ENSP00000432625.1:n.438+455T=
ENST00000533123.5:c.893T=	ENSP00000435950.1:p.Leu298=
ENST00000533196.1:n.375-48T=
ENST00000534405.5:c.893T=	ENSP00000434353.1:p.Leu298=
NM_000543.4:c.893T=	NP_000534.3:p.Leu298=
NM_001007593.2:c.890T=	NP_001007594.2:p.Leu297=
XM_005253075.3:c.893T=	XP_005253132.1:p.Leu298=
XM_011520303.1:c.893T=	XP_011518605.1:p.Leu298=
XM_011520304.1:c.893T=	XP_011518606.1:p.Leu298=
XR_930886.1:n.1191T=
NM_001318087.1:c.893T=	NP_001305016.1:p.Leu298=
NM_001318088.1:c.-69T=	NP_001305017.1:n.-69T=
NM_001365135.1:c.893T=	NP_001352064.1:p.Leu298=
NR_027400.2:n.1078T=
NR_134502.1:n.623+455T=
XM_011520304.2:c.893T=	XP_011518606.1:p.Leu298=
XR_001747940.2:n.1018T=
XR_002957158.1:n.1018T=
NM_000543.5:c.893T= MANE Select	NP_000534.3:p.Leu298=
NM_001007593.3:c.890T=	NP_001007594.2:p.Leu297=
NM_001318087.2:c.893T=	NP_001305016.1:p.Leu298=
NM_001318088.2:c.-69T=	NP_001305017.1:n.-69T=
NM_001365135.2:c.893T=	NP_001352064.1:p.Leu298=
NR_027400.3:n.1018T=
NR_134502.2:n.563+455T=