Canonical Allele Identifier: CA1950148427

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393636T= , CM000673.2:g.6393636T=	GRCh38
NC_000011.9:g.6414866T= , CM000673.1:g.6414866T=	GRCh37
NC_000011.8:g.6371442T=	NCBI36
NG_011780.1:g.8212T=
NG_029615.1:g.30779A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1283T= MANE Select	ENSP00000340409.4:p.Ile428=
ENST00000342245.8:c.1283T=	ENSP00000340409.4:p.Ile428=
ENST00000526280.1:c.340T=
ENST00000527275.5:c.1280T=	ENSP00000435350.1:p.Ile427=
ENST00000531303.5:c.*114T=	ENSP00000432625.1:n.*114T=
ENST00000531336.1:n.115T=
ENST00000532367.1:n.119T=
ENST00000533123.5:c.*10T=	ENSP00000435950.1:n.*10T=
ENST00000534405.5:c.*114T=	ENSP00000434353.1:n.*114T=
NM_000543.4:c.1283T=	NP_000534.3:p.Ile428=
NM_001007593.2:c.1280T=	NP_001007594.2:p.Ile427=
XM_005253075.3:c.1283T=	XP_005253132.1:p.Ile428=
XM_011520303.1:c.1151T=	XP_011518605.1:p.Ile384=
XM_011520304.1:c.1151T=	XP_011518606.1:p.Ile384=
XR_930886.1:n.1621T=
NM_001318087.1:c.1283T=	NP_001305016.1:p.Ile428=
NM_001318088.1:c.362T=	NP_001305017.1:p.Ile121=
NM_001365135.1:c.1151T=	NP_001352064.1:p.Ile384=
NR_027400.2:n.1296T=
NR_134502.1:n.815T=
XM_011520304.2:c.1151T=	XP_011518606.1:p.Ile384=
XR_001747940.2:n.1448T=
XR_002957158.1:n.1448T=
NM_000543.5:c.1283T= MANE Select	NP_000534.3:p.Ile428=
NM_001007593.3:c.1280T=	NP_001007594.2:p.Ile427=
NM_001318087.2:c.1283T=	NP_001305016.1:p.Ile428=
NM_001318088.2:c.362T=	NP_001305017.1:p.Ile121=
NM_001365135.2:c.1151T=	NP_001352064.1:p.Ile384=
NR_027400.3:n.1236T=
NR_134502.2:n.755T=