Canonical Allele Identifier: CA1950150277

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394623A= , CM000673.2:g.6394623A=	GRCh38
NC_000011.9:g.6415853A= , CM000673.1:g.6415853A=	GRCh37
NC_000011.8:g.6372429A=	NCBI36
NG_011780.1:g.9199A=
NG_029615.1:g.29792T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*16A= MANE Select	ENSP00000340409.4:n.*16A=
ENST00000342245.8:c.*16A=	ENSP00000340409.4:n.*16A=
ENST00000526280.1:c.969A=
ENST00000527275.5:c.*16A=	ENSP00000435350.1:n.*16A=
ENST00000531303.5:c.*763A=	ENSP00000432625.1:n.*763A=
ENST00000533123.5:c.*639A=	ENSP00000435950.1:n.*639A=
ENST00000534405.5:c.*743A=	ENSP00000434353.1:n.*743A=
NM_000543.4:c.*16A=	NP_000534.3:n.*16A=
NM_001007593.2:c.*16A=	NP_001007594.2:n.*16A=
XM_011520303.1:c.*16A=	XP_011518605.1:n.*16A=
NM_001318087.1:c.*405A=	NP_001305016.1:n.*405A=
NM_001318088.1:c.*16A=	NP_001305017.1:n.*16A=
NM_001365135.1:c.*16A=	NP_001352064.1:n.*16A=
NR_027400.2:n.1925A=
NR_134502.1:n.1464A=
XR_001747940.2:n.2097A=
XR_002957158.1:n.2279A=
NM_000543.5:c.*16A= MANE Select	NP_000534.3:n.*16A=
NM_001007593.3:c.*16A=	NP_001007594.2:n.*16A=
NM_001318087.2:c.*405A=	NP_001305016.1:n.*405A=
NM_001318088.2:c.*16A=	NP_001305017.1:n.*16A=
NM_001365135.2:c.*16A=	NP_001352064.1:n.*16A=
NR_027400.3:n.1865A=
NR_134502.2:n.1404A=