Canonical Allele Identifier: CA1950147952

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393291T= , CM000673.2:g.6393291T=	GRCh38
NC_000011.9:g.6414521T= , CM000673.1:g.6414521T=	GRCh37
NC_000011.8:g.6371097T=	NCBI36
NG_011780.1:g.7867T=
NG_029615.1:g.31124A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1167T= MANE Select	ENSP00000340409.4:p.Arg389=
ENST00000342245.8:c.1167T=	ENSP00000340409.4:p.Arg389=
ENST00000526280.1:c.321-326T=
ENST00000527275.5:c.1164T=	ENSP00000435350.1:p.Arg388=
ENST00000531303.5:c.514T=	ENSP00000432625.1:p.Ter172=
ENST00000533123.5:c.1092-326T=	ENSP00000435950.1:n.1092-326T=
ENST00000534405.5:c.1207T=	ENSP00000434353.1:p.Ter403=
NM_000543.4:c.1167T=	NP_000534.3:p.Arg389=
NM_001007593.2:c.1164T=	NP_001007594.2:p.Arg388=
XM_005253075.3:c.1167T=	XP_005253132.1:p.Arg389=
XM_011520303.1:c.1132-326T=	XP_011518605.1:n.1132-326T=
XM_011520304.1:c.1132-326T=	XP_011518606.1:n.1132-326T=
XR_930886.1:n.1505T=
NM_001318087.1:c.1167T=	NP_001305016.1:p.Arg389=
NM_001318088.1:c.246T=	NP_001305017.1:p.Arg82=
NM_001365135.1:c.1132-326T=	NP_001352064.1:n.1132-326T=
NR_027400.2:n.1277-326T=
NR_134502.1:n.699T=
XM_011520304.2:c.1132-326T=	XP_011518606.1:n.1132-326T=
XR_001747940.2:n.1332T=
XR_002957158.1:n.1332T=
NM_000543.5:c.1167T= MANE Select	NP_000534.3:p.Arg389=
NM_001007593.3:c.1164T=	NP_001007594.2:p.Arg388=
NM_001318087.2:c.1167T=	NP_001305016.1:p.Arg389=
NM_001318088.2:c.246T=	NP_001305017.1:p.Arg82=
NM_001365135.2:c.1132-326T=	NP_001352064.1:n.1132-326T=
NR_027400.3:n.1217-326T=
NR_134502.2:n.639T=