Canonical Allele Identifier: CA1950148485

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393661C= , CM000673.2:g.6393661C=	GRCh38
NC_000011.9:g.6414891C= , CM000673.1:g.6414891C=	GRCh37
NC_000011.8:g.6371467C=	NCBI36
NG_011780.1:g.8237C=
NG_029615.1:g.30754G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1308C= MANE Select	ENSP00000340409.4:p.Ser436=
ENST00000342245.8:c.1308C=	ENSP00000340409.4:p.Ser436=
ENST00000526280.1:c.365C=
ENST00000527275.5:c.1305C=	ENSP00000435350.1:p.Ser435=
ENST00000531303.5:c.*139C=	ENSP00000432625.1:n.*139C=
ENST00000531336.1:n.140C=
ENST00000532367.1:n.144C=
ENST00000533123.5:c.*35C=	ENSP00000435950.1:n.*35C=
ENST00000534405.5:c.*139C=	ENSP00000434353.1:n.*139C=
NM_000543.4:c.1308C=	NP_000534.3:p.Ser436=
NM_001007593.2:c.1305C=	NP_001007594.2:p.Ser435=
XM_005253075.3:c.1308C=	XP_005253132.1:p.Ser436=
XM_011520303.1:c.1176C=	XP_011518605.1:p.Ser392=
XM_011520304.1:c.1176C=	XP_011518606.1:p.Ser392=
XR_930886.1:n.1646C=
NM_001318087.1:c.1308C=	NP_001305016.1:p.Ser436=
NM_001318088.1:c.387C=	NP_001305017.1:p.Ser129=
NM_001365135.1:c.1176C=	NP_001352064.1:p.Ser392=
NR_027400.2:n.1321C=
NR_134502.1:n.840C=
XM_011520304.2:c.1176C=	XP_011518606.1:p.Ser392=
XR_001747940.2:n.1473C=
XR_002957158.1:n.1473C=
NM_000543.5:c.1308C= MANE Select	NP_000534.3:p.Ser436=
NM_001007593.3:c.1305C=	NP_001007594.2:p.Ser435=
NM_001318087.2:c.1308C=	NP_001305016.1:p.Ser436=
NM_001318088.2:c.387C=	NP_001305017.1:p.Ser129=
NM_001365135.2:c.1176C=	NP_001352064.1:p.Ser392=
NR_027400.3:n.1261C=
NR_134502.2:n.780C=