Canonical Allele Identifier: CA1950150564

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394925A= , CM000673.2:g.6394925A=	GRCh38
NC_000011.9:g.6416155A= , CM000673.1:g.6416155A=	GRCh37
NC_000011.8:g.6372731A=	NCBI36
NG_011780.1:g.9501A=
NG_029615.1:g.29490T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*318A= MANE Select	ENSP00000340409.4:n.*318A=
ENST00000342245.8:c.*318A=	ENSP00000340409.4:n.*318A=
ENST00000526280.1:c.1271A=
ENST00000533123.5:c.*941A=	ENSP00000435950.1:n.*941A=
ENST00000534405.5:c.*1045A=	ENSP00000434353.1:n.*1045A=
NM_000543.4:c.*318A=	NP_000534.3:n.*318A=
NM_001007593.2:c.*318A=	NP_001007594.2:n.*318A=
XM_011520303.1:c.*318A=	XP_011518605.1:n.*318A=
NM_001318087.1:c.*707A=	NP_001305016.1:n.*707A=
NM_001318088.1:c.*318A=	NP_001305017.1:n.*318A=
NM_001365135.1:c.*318A=	NP_001352064.1:n.*318A=
NR_027400.2:n.2227A=
NR_134502.1:n.1766A=
XR_001747940.2:n.2399A=
XR_002957158.1:n.2581A=
NM_000543.5:c.*318A= MANE Select	NP_000534.3:n.*318A=
NM_001007593.3:c.*318A=	NP_001007594.2:n.*318A=
NM_001318087.2:c.*707A=	NP_001305016.1:n.*707A=
NM_001318088.2:c.*318A=	NP_001305017.1:n.*318A=
NM_001365135.2:c.*318A=	NP_001352064.1:n.*318A=
NR_027400.3:n.2167A=
NR_134502.2:n.1706A=