Canonical Allele Identifier: CA1950150291

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394641T= , CM000673.2:g.6394641T=	GRCh38
NC_000011.9:g.6415871T= , CM000673.1:g.6415871T=	GRCh37
NC_000011.8:g.6372447T=	NCBI36
NG_011780.1:g.9217T=
NG_029615.1:g.29774A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*34T= MANE Select	ENSP00000340409.4:n.*34T=
ENST00000342245.8:c.*34T=	ENSP00000340409.4:n.*34T=
ENST00000526280.1:c.987T=
ENST00000527275.5:c.*34T=	ENSP00000435350.1:n.*34T=
ENST00000531303.5:c.*781T=	ENSP00000432625.1:n.*781T=
ENST00000533123.5:c.*657T=	ENSP00000435950.1:n.*657T=
ENST00000534405.5:c.*761T=	ENSP00000434353.1:n.*761T=
NM_000543.4:c.*34T=	NP_000534.3:n.*34T=
NM_001007593.2:c.*34T=	NP_001007594.2:n.*34T=
XM_011520303.1:c.*34T=	XP_011518605.1:n.*34T=
NM_001318087.1:c.*423T=	NP_001305016.1:n.*423T=
NM_001318088.1:c.*34T=	NP_001305017.1:n.*34T=
NM_001365135.1:c.*34T=	NP_001352064.1:n.*34T=
NR_027400.2:n.1943T=
NR_134502.1:n.1482T=
XR_001747940.2:n.2115T=
XR_002957158.1:n.2297T=
NM_000543.5:c.*34T= MANE Select	NP_000534.3:n.*34T=
NM_001007593.3:c.*34T=	NP_001007594.2:n.*34T=
NM_001318087.2:c.*423T=	NP_001305016.1:n.*423T=
NM_001318088.2:c.*34T=	NP_001305017.1:n.*34T=
NM_001365135.2:c.*34T=	NP_001352064.1:n.*34T=
NR_027400.3:n.1883T=
NR_134502.2:n.1422T=