Canonical Allele Identifier: CA1950150537

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394892G= , CM000673.2:g.6394892G=	GRCh38
NC_000011.9:g.6416122G= , CM000673.1:g.6416122G=	GRCh37
NC_000011.8:g.6372698G=	NCBI36
NG_011780.1:g.9468G=
NG_029615.1:g.29523C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*285G= MANE Select	ENSP00000340409.4:n.*285G=
ENST00000342245.8:c.*285G=	ENSP00000340409.4:n.*285G=
ENST00000526280.1:c.1238G=
ENST00000533123.5:c.*908G=	ENSP00000435950.1:n.*908G=
ENST00000534405.5:c.*1012G=	ENSP00000434353.1:n.*1012G=
NM_000543.4:c.*285G=	NP_000534.3:n.*285G=
NM_001007593.2:c.*285G=	NP_001007594.2:n.*285G=
XM_011520303.1:c.*285G=	XP_011518605.1:n.*285G=
NM_001318087.1:c.*674G=	NP_001305016.1:n.*674G=
NM_001318088.1:c.*285G=	NP_001305017.1:n.*285G=
NM_001365135.1:c.*285G=	NP_001352064.1:n.*285G=
NR_027400.2:n.2194G=
NR_134502.1:n.1733G=
XR_001747940.2:n.2366G=
XR_002957158.1:n.2548G=
NM_000543.5:c.*285G= MANE Select	NP_000534.3:n.*285G=
NM_001007593.3:c.*285G=	NP_001007594.2:n.*285G=
NM_001318087.2:c.*674G=	NP_001305016.1:n.*674G=
NM_001318088.2:c.*285G=	NP_001305017.1:n.*285G=
NM_001365135.2:c.*285G=	NP_001352064.1:n.*285G=
NR_027400.3:n.2134G=
NR_134502.2:n.1673G=