Canonical Allele Identifier: CA1950146429

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391986G= , CM000673.2:g.6391986G=	GRCh38
NC_000011.9:g.6413216G= , CM000673.1:g.6413216G=	GRCh37
NC_000011.8:g.6369792G=	NCBI36
NG_011780.1:g.6562G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.921G= MANE Select	ENSP00000340409.4:p.Lys307=
ENST00000342245.8:c.921G=	ENSP00000340409.4:p.Lys307=
ENST00000526280.1:c.110G=
ENST00000527275.5:c.918G=	ENSP00000435350.1:p.Lys306=
ENST00000530395.1:c.102G=	ENSP00000431479.1:p.Lys34=
ENST00000531303.5:c.438+483G=	ENSP00000432625.1:n.438+483G=
ENST00000533123.5:c.921G=	ENSP00000435950.1:p.Lys307=
ENST00000533196.1:n.375-20G=
ENST00000534405.5:c.921G=	ENSP00000434353.1:p.Lys307=
NM_000543.4:c.921G=	NP_000534.3:p.Lys307=
NM_001007593.2:c.918G=	NP_001007594.2:p.Lys306=
XM_005253075.3:c.921G=	XP_005253132.1:p.Lys307=
XM_011520303.1:c.921G=	XP_011518605.1:p.Lys307=
XM_011520304.1:c.921G=	XP_011518606.1:p.Lys307=
XR_930886.1:n.1219G=
NM_001318087.1:c.921G=	NP_001305016.1:p.Lys307=
NM_001318088.1:c.-41G=	NP_001305017.1:n.-41G=
NM_001365135.1:c.921G=	NP_001352064.1:p.Lys307=
NR_027400.2:n.1106G=
NR_134502.1:n.623+483G=
XM_011520304.2:c.921G=	XP_011518606.1:p.Lys307=
XR_001747940.2:n.1046G=
XR_002957158.1:n.1046G=
NM_000543.5:c.921G= MANE Select	NP_000534.3:p.Lys307=
NM_001007593.3:c.918G=	NP_001007594.2:p.Lys306=
NM_001318087.2:c.921G=	NP_001305016.1:p.Lys307=
NM_001318088.2:c.-41G=	NP_001305017.1:n.-41G=
NM_001365135.2:c.921G=	NP_001352064.1:p.Lys307=
NR_027400.3:n.1046G=
NR_134502.2:n.563+483G=