Canonical Allele Identifier: CA1950146197

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6391572C= , CM000673.2:g.6391572C=	GRCh38
NC_000011.9:g.6412802C= , CM000673.1:g.6412802C=	GRCh37
NC_000011.8:g.6369378C=	NCBI36
NG_011780.1:g.6148C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.507C= MANE Select	ENSP00000340409.4:p.His169=
ENST00000342245.8:c.507C=	ENSP00000340409.4:p.His169=
ENST00000527275.5:c.504C=	ENSP00000435350.1:p.His168=
ENST00000530395.1:c.-95-218C=	ENSP00000431479.1:n.-95-218C=
ENST00000531303.5:c.438+69C=	ENSP00000432625.1:n.438+69C=
ENST00000533123.5:c.507C=	ENSP00000435950.1:p.His169=
ENST00000533196.1:n.375-434C=
ENST00000534405.5:c.507C=	ENSP00000434353.1:p.His169=
NM_000543.4:c.507C=	NP_000534.3:p.His169=
NM_001007593.2:c.504C=	NP_001007594.2:p.His168=
XM_005253075.3:c.507C=	XP_005253132.1:p.His169=
XM_011520303.1:c.507C=	XP_011518605.1:p.His169=
XM_011520304.1:c.507C=	XP_011518606.1:p.His169=
XR_930886.1:n.805C=
NM_001318087.1:c.507C=	NP_001305016.1:p.His169=
NM_001318088.1:c.-455C=	NP_001305017.1:n.-455C=
NM_001365135.1:c.507C=	NP_001352064.1:p.His169=
NR_027400.2:n.692C=
NR_134502.1:n.623+69C=
XM_011520304.2:c.507C=	XP_011518606.1:p.His169=
XR_001747940.2:n.632C=
XR_002957158.1:n.632C=
NM_000543.5:c.507C= MANE Select	NP_000534.3:p.His169=
NM_001007593.3:c.504C=	NP_001007594.2:p.His168=
NM_001318087.2:c.507C=	NP_001305016.1:p.His169=
NM_001318088.2:c.-455C=	NP_001305017.1:n.-455C=
NM_001365135.2:c.507C=	NP_001352064.1:p.His169=
NR_027400.3:n.632C=
NR_134502.2:n.563+69C=