Canonical Allele Identifier: CA1950150338

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394691G= , CM000673.2:g.6394691G=	GRCh38
NC_000011.9:g.6415921G= , CM000673.1:g.6415921G=	GRCh37
NC_000011.8:g.6372497G=	NCBI36
NG_011780.1:g.9267G=
NG_029615.1:g.29724C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*84G= MANE Select	ENSP00000340409.4:n.*84G=
ENST00000342245.8:c.*84G=	ENSP00000340409.4:n.*84G=
ENST00000526280.1:c.1037G=
ENST00000527275.5:c.*84G=	ENSP00000435350.1:n.*84G=
ENST00000531303.5:c.*831G=	ENSP00000432625.1:n.*831G=
ENST00000533123.5:c.*707G=	ENSP00000435950.1:n.*707G=
ENST00000534405.5:c.*811G=	ENSP00000434353.1:n.*811G=
NM_000543.4:c.*84G=	NP_000534.3:n.*84G=
NM_001007593.2:c.*84G=	NP_001007594.2:n.*84G=
XM_011520303.1:c.*84G=	XP_011518605.1:n.*84G=
NM_001318087.1:c.*473G=	NP_001305016.1:n.*473G=
NM_001318088.1:c.*84G=	NP_001305017.1:n.*84G=
NM_001365135.1:c.*84G=	NP_001352064.1:n.*84G=
NR_027400.2:n.1993G=
NR_134502.1:n.1532G=
XR_001747940.2:n.2165G=
XR_002957158.1:n.2347G=
NM_000543.5:c.*84G= MANE Select	NP_000534.3:n.*84G=
NM_001007593.3:c.*84G=	NP_001007594.2:n.*84G=
NM_001318087.2:c.*473G=	NP_001305016.1:n.*473G=
NM_001318088.2:c.*84G=	NP_001305017.1:n.*84G=
NM_001365135.2:c.*84G=	NP_001352064.1:n.*84G=
NR_027400.3:n.1933G=
NR_134502.2:n.1472G=