Canonical Allele Identifier: CA1950147891

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393272A= , CM000673.2:g.6393272A=	GRCh38
NC_000011.9:g.6414502A= , CM000673.1:g.6414502A=	GRCh37
NC_000011.8:g.6371078A=	NCBI36
NG_011780.1:g.7848A=
NG_029615.1:g.31143T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1148A= MANE Select	ENSP00000340409.4:p.Asn383=
ENST00000342245.8:c.1148A=	ENSP00000340409.4:p.Asn383=
ENST00000526280.1:c.321-345A=
ENST00000527275.5:c.1145A=	ENSP00000435350.1:p.Asn382=
ENST00000531303.5:c.495A=	ENSP00000432625.1:p.Gln165=
ENST00000533123.5:c.1092-345A=	ENSP00000435950.1:n.1092-345A=
ENST00000534405.5:c.1188A=	ENSP00000434353.1:p.Gln396=
NM_000543.4:c.1148A=	NP_000534.3:p.Asn383=
NM_001007593.2:c.1145A=	NP_001007594.2:p.Asn382=
XM_005253075.3:c.1148A=	XP_005253132.1:p.Asn383=
XM_011520303.1:c.1132-345A=	XP_011518605.1:n.1132-345A=
XM_011520304.1:c.1132-345A=	XP_011518606.1:n.1132-345A=
XR_930886.1:n.1486A=
NM_001318087.1:c.1148A=	NP_001305016.1:p.Asn383=
NM_001318088.1:c.227A=	NP_001305017.1:p.Asn76=
NM_001365135.1:c.1132-345A=	NP_001352064.1:n.1132-345A=
NR_027400.2:n.1277-345A=
NR_134502.1:n.680A=
XM_011520304.2:c.1132-345A=	XP_011518606.1:n.1132-345A=
XR_001747940.2:n.1313A=
XR_002957158.1:n.1313A=
NM_000543.5:c.1148A= MANE Select	NP_000534.3:p.Asn383=
NM_001007593.3:c.1145A=	NP_001007594.2:p.Asn382=
NM_001318087.2:c.1148A=	NP_001305016.1:p.Asn383=
NM_001318088.2:c.227A=	NP_001305017.1:p.Asn76=
NM_001365135.2:c.1132-345A=	NP_001352064.1:n.1132-345A=
NR_027400.3:n.1217-345A=
NR_134502.2:n.620A=