Canonical Allele Identifier: CA1950150286

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394635T= , CM000673.2:g.6394635T=	GRCh38
NC_000011.9:g.6415865T= , CM000673.1:g.6415865T=	GRCh37
NC_000011.8:g.6372441T=	NCBI36
NG_011780.1:g.9211T=
NG_029615.1:g.29780A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*28T= MANE Select	ENSP00000340409.4:n.*28T=
ENST00000342245.8:c.*28T=	ENSP00000340409.4:n.*28T=
ENST00000526280.1:c.981T=
ENST00000527275.5:c.*28T=	ENSP00000435350.1:n.*28T=
ENST00000531303.5:c.*775T=	ENSP00000432625.1:n.*775T=
ENST00000533123.5:c.*651T=	ENSP00000435950.1:n.*651T=
ENST00000534405.5:c.*755T=	ENSP00000434353.1:n.*755T=
NM_000543.4:c.*28T=	NP_000534.3:n.*28T=
NM_001007593.2:c.*28T=	NP_001007594.2:n.*28T=
XM_011520303.1:c.*28T=	XP_011518605.1:n.*28T=
NM_001318087.1:c.*417T=	NP_001305016.1:n.*417T=
NM_001318088.1:c.*28T=	NP_001305017.1:n.*28T=
NM_001365135.1:c.*28T=	NP_001352064.1:n.*28T=
NR_027400.2:n.1937T=
NR_134502.1:n.1476T=
XR_001747940.2:n.2109T=
XR_002957158.1:n.2291T=
NM_000543.5:c.*28T= MANE Select	NP_000534.3:n.*28T=
NM_001007593.3:c.*28T=	NP_001007594.2:n.*28T=
NM_001318087.2:c.*417T=	NP_001305016.1:n.*417T=
NM_001318088.2:c.*28T=	NP_001305017.1:n.*28T=
NM_001365135.2:c.*28T=	NP_001352064.1:n.*28T=
NR_027400.3:n.1877T=
NR_134502.2:n.1416T=