Canonical Allele Identifier: CA1950146439

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6392002C= , CM000673.2:g.6392002C=	GRCh38
NC_000011.9:g.6413232C= , CM000673.1:g.6413232C=	GRCh37
NC_000011.8:g.6369808C=	NCBI36
NG_011780.1:g.6578C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.937C= MANE Select	ENSP00000340409.4:p.Pro313=
ENST00000342245.8:c.937C=	ENSP00000340409.4:p.Pro313=
ENST00000526280.1:c.126C=
ENST00000527275.5:c.934C=	ENSP00000435350.1:p.Pro312=
ENST00000530395.1:c.118C=	ENSP00000431479.1:p.Pro40=
ENST00000531303.5:c.438+499C=	ENSP00000432625.1:n.438+499C=
ENST00000533123.5:c.937C=	ENSP00000435950.1:p.Pro313=
ENST00000533196.1:n.375-4C=
ENST00000534405.5:c.937C=	ENSP00000434353.1:p.Pro313=
NM_000543.4:c.937C=	NP_000534.3:p.Pro313=
NM_001007593.2:c.934C=	NP_001007594.2:p.Pro312=
XM_005253075.3:c.937C=	XP_005253132.1:p.Pro313=
XM_011520303.1:c.937C=	XP_011518605.1:p.Pro313=
XM_011520304.1:c.937C=	XP_011518606.1:p.Pro313=
XR_930886.1:n.1235C=
NM_001318087.1:c.937C=	NP_001305016.1:p.Pro313=
NM_001318088.1:c.-25C=	NP_001305017.1:n.-25C=
NM_001365135.1:c.937C=	NP_001352064.1:p.Pro313=
NR_027400.2:n.1122C=
NR_134502.1:n.623+499C=
XM_011520304.2:c.937C=	XP_011518606.1:p.Pro313=
XR_001747940.2:n.1062C=
XR_002957158.1:n.1062C=
NM_000543.5:c.937C= MANE Select	NP_000534.3:p.Pro313=
NM_001007593.3:c.934C=	NP_001007594.2:p.Pro312=
NM_001318087.2:c.937C=	NP_001305016.1:p.Pro313=
NM_001318088.2:c.-25C=	NP_001305017.1:n.-25C=
NM_001365135.2:c.937C=	NP_001352064.1:p.Pro313=
NR_027400.3:n.1062C=
NR_134502.2:n.563+499C=