Canonical Allele Identifier: CA1950149469

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394251C= , CM000673.2:g.6394251C=	GRCh38
NC_000011.9:g.6415481C= , CM000673.1:g.6415481C=	GRCh37
NC_000011.8:g.6372057C=	NCBI36
NG_011780.1:g.8827C=
NG_029615.1:g.30164G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1540C= MANE Select	ENSP00000340409.4:p.Leu514=
ENST00000342245.8:c.1540C=	ENSP00000340409.4:p.Leu514=
ENST00000526280.1:c.597C=
ENST00000527275.5:c.1537C=	ENSP00000435350.1:p.Leu513=
ENST00000531303.5:c.*391C=	ENSP00000432625.1:n.*391C=
ENST00000531336.1:n.528C=
ENST00000533123.5:c.*267C=	ENSP00000435950.1:n.*267C=
ENST00000534405.5:c.*371C=	ENSP00000434353.1:n.*371C=
NM_000543.4:c.1540C=	NP_000534.3:p.Leu514=
NM_001007593.2:c.1537C=	NP_001007594.2:p.Leu513=
XM_005253075.3:c.*33C=	XP_005253132.1:n.*33C=
XM_011520303.1:c.1408C=	XP_011518605.1:p.Leu470=
XM_011520304.1:c.*33C=	XP_011518606.1:n.*33C=
NM_001318087.1:c.*33C=	NP_001305016.1:n.*33C=
NM_001318088.1:c.619C=	NP_001305017.1:p.Leu207=
NM_001365135.1:c.1408C=	NP_001352064.1:p.Leu470=
NR_027400.2:n.1553C=
NR_134502.1:n.1092C=
XM_011520304.2:c.*33C=	XP_011518606.1:n.*33C=
XR_001747940.2:n.1725C=
XR_002957158.1:n.1907C=
NM_000543.5:c.1540C= MANE Select	NP_000534.3:p.Leu514=
NM_001007593.3:c.1537C=	NP_001007594.2:p.Leu513=
NM_001318087.2:c.*33C=	NP_001305016.1:n.*33C=
NM_001318088.2:c.619C=	NP_001305017.1:p.Leu207=
NM_001365135.2:c.1408C=	NP_001352064.1:p.Leu470=
NR_027400.3:n.1493C=
NR_134502.2:n.1032C=