Canonical Allele Identifier: CA1950146525

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392091G= , CM000673.2:g.6392091G=	GRCh38
NC_000011.9:g.6413321G= , CM000673.1:g.6413321G=	GRCh37
NC_000011.8:g.6369897G=	NCBI36
NG_011780.1:g.6667G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1026G= MANE Select	ENSP00000340409.4:p.Trp342=
ENST00000342245.8:c.1026G=	ENSP00000340409.4:p.Trp342=
ENST00000526280.1:c.215G=
ENST00000527275.5:c.1023G=	ENSP00000435350.1:p.Trp341=
ENST00000531303.5:c.438+588G=	ENSP00000432625.1:n.438+588G=
ENST00000533123.5:c.1026G=	ENSP00000435950.1:p.Trp342=
ENST00000534405.5:c.1026G=	ENSP00000434353.1:p.Trp342=
NM_000543.4:c.1026G=	NP_000534.3:p.Trp342=
NM_001007593.2:c.1023G=	NP_001007594.2:p.Trp341=
XM_005253075.3:c.1026G=	XP_005253132.1:p.Trp342=
XM_011520303.1:c.1026G=	XP_011518605.1:p.Trp342=
XM_011520304.1:c.1026G=	XP_011518606.1:p.Trp342=
XR_930886.1:n.1324G=
NM_001318087.1:c.1026G=	NP_001305016.1:p.Trp342=
NM_001318088.1:c.65G=	NP_001305017.1:p.Gly22=
NM_001365135.1:c.1026G=	NP_001352064.1:p.Trp342=
NR_027400.2:n.1211G=
NR_134502.1:n.623+588G=
XM_011520304.2:c.1026G=	XP_011518606.1:p.Trp342=
XR_001747940.2:n.1151G=
XR_002957158.1:n.1151G=
NM_000543.5:c.1026G= MANE Select	NP_000534.3:p.Trp342=
NM_001007593.3:c.1023G=	NP_001007594.2:p.Trp341=
NM_001318087.2:c.1026G=	NP_001305016.1:p.Trp342=
NM_001318088.2:c.65G=	NP_001305017.1:p.Gly22=
NM_001365135.2:c.1026G=	NP_001352064.1:p.Trp342=
NR_027400.3:n.1151G=
NR_134502.2:n.563+588G=