Canonical Allele Identifier: CA1950149291

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394177G= , CM000673.2:g.6394177G=	GRCh38
NC_000011.9:g.6415407G= , CM000673.1:g.6415407G=	GRCh37
NC_000011.8:g.6371983G=	NCBI36
NG_011780.1:g.8753G=
NG_029615.1:g.30238C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1487-21G= MANE Select	ENSP00000340409.4:n.1487-21G=
ENST00000342245.8:c.1487-21G=	ENSP00000340409.4:n.1487-21G=
ENST00000526280.1:c.544-21G=
ENST00000527275.5:c.1484-21G=	ENSP00000435350.1:n.1484-21G=
ENST00000531303.5:c.*318-1G=	ENSP00000432625.1:n.*318-1G=
ENST00000531336.1:n.454G=
ENST00000533123.5:c.*214-21G=	ENSP00000435950.1:n.*214-21G=
ENST00000534405.5:c.*318-21G=	ENSP00000434353.1:n.*318-21G=
NM_000543.4:c.1487-21G=	NP_000534.3:n.1487-21G=
NM_001007593.2:c.1484-21G=	NP_001007594.2:n.1484-21G=
XM_005253075.3:c.1487-1G=	XP_005253132.1:n.1487-1G=
XM_011520303.1:c.1355-21G=	XP_011518605.1:n.1355-21G=
XM_011520304.1:c.1355-1G=	XP_011518606.1:n.1355-1G=
NM_001318087.1:c.1487-1G=	NP_001305016.1:n.1487-1G=
NM_001318088.1:c.566-21G=	NP_001305017.1:n.566-21G=
NM_001365135.1:c.1355-21G=	NP_001352064.1:n.1355-21G=
NR_027400.2:n.1500-21G=
NR_134502.1:n.1019-1G=
XM_011520304.2:c.1355-1G=	XP_011518606.1:n.1355-1G=
XR_001747940.2:n.1652-1G=
XR_002957158.1:n.1854-21G=
NM_000543.5:c.1487-21G= MANE Select	NP_000534.3:n.1487-21G=
NM_001007593.3:c.1484-21G=	NP_001007594.2:n.1484-21G=
NM_001318087.2:c.1487-1G=	NP_001305016.1:n.1487-1G=
NM_001318088.2:c.566-21G=	NP_001305017.1:n.566-21G=
NM_001365135.2:c.1355-21G=	NP_001352064.1:n.1355-21G=
NR_027400.3:n.1440-21G=
NR_134502.2:n.959-1G=