Canonical Allele Identifier: CA1950150400

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394740A= , CM000673.2:g.6394740A=	GRCh38
NC_000011.9:g.6415970A= , CM000673.1:g.6415970A=	GRCh37
NC_000011.8:g.6372546A=	NCBI36
NG_011780.1:g.9316A=
NG_029615.1:g.29675T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*133A= MANE Select	ENSP00000340409.4:n.*133A=
ENST00000342245.8:c.*133A=	ENSP00000340409.4:n.*133A=
ENST00000526280.1:c.1086A=
ENST00000527275.5:c.*133A=	ENSP00000435350.1:n.*133A=
ENST00000531303.5:c.*880A=	ENSP00000432625.1:n.*880A=
ENST00000533123.5:c.*756A=	ENSP00000435950.1:n.*756A=
ENST00000534405.5:c.*860A=	ENSP00000434353.1:n.*860A=
NM_000543.4:c.*133A=	NP_000534.3:n.*133A=
NM_001007593.2:c.*133A=	NP_001007594.2:n.*133A=
XM_011520303.1:c.*133A=	XP_011518605.1:n.*133A=
NM_001318087.1:c.*522A=	NP_001305016.1:n.*522A=
NM_001318088.1:c.*133A=	NP_001305017.1:n.*133A=
NM_001365135.1:c.*133A=	NP_001352064.1:n.*133A=
NR_027400.2:n.2042A=
NR_134502.1:n.1581A=
XR_001747940.2:n.2214A=
XR_002957158.1:n.2396A=
NM_000543.5:c.*133A= MANE Select	NP_000534.3:n.*133A=
NM_001007593.3:c.*133A=	NP_001007594.2:n.*133A=
NM_001318087.2:c.*522A=	NP_001305016.1:n.*522A=
NM_001318088.2:c.*133A=	NP_001305017.1:n.*133A=
NM_001365135.2:c.*133A=	NP_001352064.1:n.*133A=
NR_027400.3:n.1982A=
NR_134502.2:n.1521A=