Canonical Allele Identifier: CA1950146728

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392265T= , CM000673.2:g.6392265T=	GRCh38
NC_000011.9:g.6413495T= , CM000673.1:g.6413495T=	GRCh37
NC_000011.8:g.6370071T=	NCBI36
NG_011780.1:g.6841T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1091+109T= MANE Select	ENSP00000340409.4:n.1091+109T=
ENST00000342245.8:c.1091+109T=	ENSP00000340409.4:n.1091+109T=
ENST00000526280.1:c.320+69T=
ENST00000527275.5:c.1088+109T=	ENSP00000435350.1:n.1088+109T=
ENST00000531303.5:c.438+762T=	ENSP00000432625.1:n.438+762T=
ENST00000533123.5:c.1091+109T=	ENSP00000435950.1:n.1091+109T=
ENST00000534405.5:c.1131+69T=	ENSP00000434353.1:n.1131+69T=
NM_000543.4:c.1091+109T=	NP_000534.3:n.1091+109T=
NM_001007593.2:c.1088+109T=	NP_001007594.2:n.1088+109T=
XM_005253075.3:c.1091+109T=	XP_005253132.1:n.1091+109T=
XM_011520303.1:c.1131+69T=	XP_011518605.1:n.1131+69T=
XM_011520304.1:c.1131+69T=	XP_011518606.1:n.1131+69T=
XR_930886.1:n.1429+69T=
NM_001318087.1:c.1091+109T=	NP_001305016.1:n.1091+109T=
NM_001318088.1:c.170+69T=	NP_001305017.1:n.170+69T=
NM_001365135.1:c.1131+69T=	NP_001352064.1:n.1131+69T=
NR_027400.2:n.1276+109T=
NR_134502.1:n.623+762T=
XM_011520304.2:c.1131+69T=	XP_011518606.1:n.1131+69T=
XR_001747940.2:n.1256+69T=
XR_002957158.1:n.1256+69T=
NM_000543.5:c.1091+109T= MANE Select	NP_000534.3:n.1091+109T=
NM_001007593.3:c.1088+109T=	NP_001007594.2:n.1088+109T=
NM_001318087.2:c.1091+109T=	NP_001305016.1:n.1091+109T=
NM_001318088.2:c.170+69T=	NP_001305017.1:n.170+69T=
NM_001365135.2:c.1131+69T=	NP_001352064.1:n.1131+69T=
NR_027400.3:n.1216+109T=
NR_134502.2:n.563+762T=