Canonical Allele Identifier: CA1950148466

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393650T= , CM000673.2:g.6393650T=	GRCh38
NC_000011.9:g.6414880T= , CM000673.1:g.6414880T=	GRCh37
NC_000011.8:g.6371456T=	NCBI36
NG_011780.1:g.8226T=
NG_029615.1:g.30765A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1297T= MANE Select	ENSP00000340409.4:p.Cys433=
ENST00000342245.8:c.1297T=	ENSP00000340409.4:p.Cys433=
ENST00000526280.1:c.354T=
ENST00000527275.5:c.1294T=	ENSP00000435350.1:p.Cys432=
ENST00000531303.5:c.*128T=	ENSP00000432625.1:n.*128T=
ENST00000531336.1:n.129T=
ENST00000532367.1:n.133T=
ENST00000533123.5:c.*24T=	ENSP00000435950.1:n.*24T=
ENST00000534405.5:c.*128T=	ENSP00000434353.1:n.*128T=
NM_000543.4:c.1297T=	NP_000534.3:p.Cys433=
NM_001007593.2:c.1294T=	NP_001007594.2:p.Cys432=
XM_005253075.3:c.1297T=	XP_005253132.1:p.Cys433=
XM_011520303.1:c.1165T=	XP_011518605.1:p.Cys389=
XM_011520304.1:c.1165T=	XP_011518606.1:p.Cys389=
XR_930886.1:n.1635T=
NM_001318087.1:c.1297T=	NP_001305016.1:p.Cys433=
NM_001318088.1:c.376T=	NP_001305017.1:p.Cys126=
NM_001365135.1:c.1165T=	NP_001352064.1:p.Cys389=
NR_027400.2:n.1310T=
NR_134502.1:n.829T=
XM_011520304.2:c.1165T=	XP_011518606.1:p.Cys389=
XR_001747940.2:n.1462T=
XR_002957158.1:n.1462T=
NM_000543.5:c.1297T= MANE Select	NP_000534.3:p.Cys433=
NM_001007593.3:c.1294T=	NP_001007594.2:p.Cys432=
NM_001318087.2:c.1297T=	NP_001305016.1:p.Cys433=
NM_001318088.2:c.376T=	NP_001305017.1:p.Cys126=
NM_001365135.2:c.1165T=	NP_001352064.1:p.Cys389=
NR_027400.3:n.1250T=
NR_134502.2:n.769T=