Canonical Allele Identifier: CA1950148449

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393647C= , CM000673.2:g.6393647C=	GRCh38
NC_000011.9:g.6414877C= , CM000673.1:g.6414877C=	GRCh37
NC_000011.8:g.6371453C=	NCBI36
NG_011780.1:g.8223C=
NG_029615.1:g.30768G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1294C= MANE Select	ENSP00000340409.4:p.His432=
ENST00000342245.8:c.1294C=	ENSP00000340409.4:p.His432=
ENST00000526280.1:c.351C=
ENST00000527275.5:c.1291C=	ENSP00000435350.1:p.His431=
ENST00000531303.5:c.*125C=	ENSP00000432625.1:n.*125C=
ENST00000531336.1:n.126C=
ENST00000532367.1:n.130C=
ENST00000533123.5:c.*21C=	ENSP00000435950.1:n.*21C=
ENST00000534405.5:c.*125C=	ENSP00000434353.1:n.*125C=
NM_000543.4:c.1294C=	NP_000534.3:p.His432=
NM_001007593.2:c.1291C=	NP_001007594.2:p.His431=
XM_005253075.3:c.1294C=	XP_005253132.1:p.His432=
XM_011520303.1:c.1162C=	XP_011518605.1:p.His388=
XM_011520304.1:c.1162C=	XP_011518606.1:p.His388=
XR_930886.1:n.1632C=
NM_001318087.1:c.1294C=	NP_001305016.1:p.His432=
NM_001318088.1:c.373C=	NP_001305017.1:p.His125=
NM_001365135.1:c.1162C=	NP_001352064.1:p.His388=
NR_027400.2:n.1307C=
NR_134502.1:n.826C=
XM_011520304.2:c.1162C=	XP_011518606.1:p.His388=
XR_001747940.2:n.1459C=
XR_002957158.1:n.1459C=
NM_000543.5:c.1294C= MANE Select	NP_000534.3:p.His432=
NM_001007593.3:c.1291C=	NP_001007594.2:p.His431=
NM_001318087.2:c.1294C=	NP_001305016.1:p.His432=
NM_001318088.2:c.373C=	NP_001305017.1:p.His125=
NM_001365135.2:c.1162C=	NP_001352064.1:p.His388=
NR_027400.3:n.1247C=
NR_134502.2:n.766C=