Canonical Allele Identifier: CA1950146949

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392455C= , CM000673.2:g.6392455C=	GRCh38
NC_000011.9:g.6413685C= , CM000673.1:g.6413685C=	GRCh37
NC_000011.8:g.6370261C=	NCBI36
NG_011780.1:g.7031C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1091+299C= MANE Select	ENSP00000340409.4:n.1091+299C=
ENST00000342245.8:c.1091+299C=	ENSP00000340409.4:n.1091+299C=
ENST00000526280.1:c.320+259C=
ENST00000527275.5:c.1088+299C=	ENSP00000435350.1:n.1088+299C=
ENST00000531303.5:c.439-761C=	ENSP00000432625.1:n.439-761C=
ENST00000533123.5:c.1091+299C=	ENSP00000435950.1:n.1091+299C=
ENST00000534405.5:c.1131+259C=	ENSP00000434353.1:n.1131+259C=
NM_000543.4:c.1091+299C=	NP_000534.3:n.1091+299C=
NM_001007593.2:c.1088+299C=	NP_001007594.2:n.1088+299C=
XM_005253075.3:c.1091+299C=	XP_005253132.1:n.1091+299C=
XM_011520303.1:c.1131+259C=	XP_011518605.1:n.1131+259C=
XM_011520304.1:c.1131+259C=	XP_011518606.1:n.1131+259C=
XR_930886.1:n.1429+259C=
NM_001318087.1:c.1091+299C=	NP_001305016.1:n.1091+299C=
NM_001318088.1:c.170+259C=	NP_001305017.1:n.170+259C=
NM_001365135.1:c.1131+259C=	NP_001352064.1:n.1131+259C=
NR_027400.2:n.1276+299C=
NR_134502.1:n.624-761C=
XM_011520304.2:c.1131+259C=	XP_011518606.1:n.1131+259C=
XR_001747940.2:n.1256+259C=
XR_002957158.1:n.1256+259C=
NM_000543.5:c.1091+299C= MANE Select	NP_000534.3:n.1091+299C=
NM_001007593.3:c.1088+299C=	NP_001007594.2:n.1088+299C=
NM_001318087.2:c.1091+299C=	NP_001305016.1:n.1091+299C=
NM_001318088.2:c.170+259C=	NP_001305017.1:n.170+259C=
NM_001365135.2:c.1131+259C=	NP_001352064.1:n.1131+259C=
NR_027400.3:n.1216+299C=
NR_134502.2:n.564-761C=