Canonical Allele Identifier: CA1950145537

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6390486A= , CM000673.2:g.6390486A=	GRCh38
NC_000011.9:g.6411716A= , CM000673.1:g.6411716A=	GRCh37
NC_000011.8:g.6368292A=	NCBI36
NG_011780.1:g.5062A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.-113A= MANE Select	ENSP00000340409.4:n.-113A=
ENST00000342245.8:c.-113A=	ENSP00000340409.4:n.-113A=
ENST00000527275.5:c.-113A=	ENSP00000435350.1:n.-113A=
ENST00000530395.1:c.-249A=	ENSP00000431479.1:n.-249A=
ENST00000533196.1:n.47A=
ENST00000534405.5:c.-113A=	ENSP00000434353.1:n.-113A=
NM_000543.4:c.-113A=	NP_000534.3:n.-113A=
NM_001007593.2:c.-113A=	NP_001007594.2:n.-113A=
XM_005253075.3:c.-113A=	XP_005253132.1:n.-113A=
XM_011520303.1:c.-113A=	XP_011518605.1:n.-113A=
XM_011520304.1:c.-113A=	XP_011518606.1:n.-113A=
XR_930886.1:n.186A=
NM_001318087.1:c.-113A=	NP_001305016.1:n.-113A=
NM_001318088.1:c.-1074A=	NP_001305017.1:n.-1074A=
NM_001365135.1:c.-113A=	NP_001352064.1:n.-113A=
NR_027400.2:n.73A=
NR_134502.1:n.73A=
XM_011520304.2:c.-113A=	XP_011518606.1:n.-113A=
XR_001747940.2:n.13A=
XR_002957158.1:n.13A=
NM_000543.5:c.-113A= MANE Select	NP_000534.3:n.-113A=
NM_001007593.3:c.-113A=	NP_001007594.2:n.-113A=
NM_001318087.2:c.-113A=	NP_001305016.1:n.-113A=
NM_001318088.2:c.-1074A=	NP_001305017.1:n.-1074A=
NM_001365135.2:c.-113A=	NP_001352064.1:n.-113A=
NR_027400.3:n.13A=
NR_134502.2:n.13A=