Canonical Allele Identifier: CA1950149501

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394263A= , CM000673.2:g.6394263A=	GRCh38
NC_000011.9:g.6415493A= , CM000673.1:g.6415493A=	GRCh37
NC_000011.8:g.6372069A=	NCBI36
NG_011780.1:g.8839A=
NG_029615.1:g.30152T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1552A= MANE Select	ENSP00000340409.4:p.Thr518=
ENST00000342245.8:c.1552A=	ENSP00000340409.4:p.Thr518=
ENST00000526280.1:c.609A=
ENST00000527275.5:c.1549A=	ENSP00000435350.1:p.Thr517=
ENST00000531303.5:c.*403A=	ENSP00000432625.1:n.*403A=
ENST00000531336.1:n.540A=
ENST00000533123.5:c.*279A=	ENSP00000435950.1:n.*279A=
ENST00000534405.5:c.*383A=	ENSP00000434353.1:n.*383A=
NM_000543.4:c.1552A=	NP_000534.3:p.Thr518=
NM_001007593.2:c.1549A=	NP_001007594.2:p.Thr517=
XM_005253075.3:c.*45A=	XP_005253132.1:n.*45A=
XM_011520303.1:c.1420A=	XP_011518605.1:p.Thr474=
XM_011520304.1:c.*45A=	XP_011518606.1:n.*45A=
NM_001318087.1:c.*45A=	NP_001305016.1:n.*45A=
NM_001318088.1:c.631A=	NP_001305017.1:p.Thr211=
NM_001365135.1:c.1420A=	NP_001352064.1:p.Thr474=
NR_027400.2:n.1565A=
NR_134502.1:n.1104A=
XM_011520304.2:c.*45A=	XP_011518606.1:n.*45A=
XR_001747940.2:n.1737A=
XR_002957158.1:n.1919A=
NM_000543.5:c.1552A= MANE Select	NP_000534.3:p.Thr518=
NM_001007593.3:c.1549A=	NP_001007594.2:p.Thr517=
NM_001318087.2:c.*45A=	NP_001305016.1:n.*45A=
NM_001318088.2:c.631A=	NP_001305017.1:p.Thr211=
NM_001365135.2:c.1420A=	NP_001352064.1:p.Thr474=
NR_027400.3:n.1505A=
NR_134502.2:n.1044A=