Canonical Allele Identifier: CA217301993

Gene: SMPD1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393655G>A , CM000673.2:g.6393655G>A	GRCh38
NC_000011.9:g.6414885G>A , CM000673.1:g.6414885G>A	GRCh37
NC_000011.8:g.6371461G>A	NCBI36
NG_011780.1:g.8231G>A
NG_029615.1:g.30760C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1302G>A MANE Select	ENSP00000340409.4:p.Leu434=
ENST00000342245.8:c.1302G>A	ENSP00000340409.4:p.Leu434=
ENST00000526280.1:c.359G>A
ENST00000527275.5:c.1299G>A	ENSP00000435350.1:p.Leu433=
ENST00000531303.5:c.*133G>A	ENSP00000432625.1:n.*133G>A
ENST00000531336.1:n.134G>A
ENST00000532367.1:n.138G>A
ENST00000533123.5:c.*29G>A	ENSP00000435950.1:n.*29G>A
ENST00000534405.5:c.*133G>A	ENSP00000434353.1:n.*133G>A
NM_000543.4:c.1302G>A	NP_000534.3:p.Leu434=
NM_001007593.2:c.1299G>A	NP_001007594.2:p.Leu433=
XM_005253075.3:c.1302G>A	XP_005253132.1:p.Leu434=
XM_011520303.1:c.1170G>A	XP_011518605.1:p.Leu390=
XM_011520304.1:c.1170G>A	XP_011518606.1:p.Leu390=
XR_930886.1:n.1640G>A
NM_001318087.1:c.1302G>A	NP_001305016.1:p.Leu434=
NM_001318088.1:c.381G>A	NP_001305017.1:p.Leu127=
NM_001365135.1:c.1170G>A	NP_001352064.1:p.Leu390=
NR_027400.2:n.1315G>A
NR_134502.1:n.834G>A
XM_011520304.2:c.1170G>A	XP_011518606.1:p.Leu390=
XR_001747940.2:n.1467G>A
XR_002957158.1:n.1467G>A
NM_000543.5:c.1302G>A MANE Select	NP_000534.3:p.Leu434=
NM_001007593.3:c.1299G>A	NP_001007594.2:p.Leu433=
NM_001318087.2:c.1302G>A	NP_001305016.1:p.Leu434=
NM_001318088.2:c.381G>A	NP_001305017.1:p.Leu127=
NM_001365135.2:c.1170G>A	NP_001352064.1:p.Leu390=
NR_027400.3:n.1255G>A
NR_134502.2:n.774G>A