Canonical Allele Identifier: CA1950148541

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393685T= , CM000673.2:g.6393685T=	GRCh38
NC_000011.9:g.6414915T= , CM000673.1:g.6414915T=	GRCh37
NC_000011.8:g.6371491T=	NCBI36
NG_011780.1:g.8261T=
NG_029615.1:g.30730A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1332T= MANE Select	ENSP00000340409.4:p.Ile444=
ENST00000342245.8:c.1332T=	ENSP00000340409.4:p.Ile444=
ENST00000526280.1:c.389T=
ENST00000527275.5:c.1329T=	ENSP00000435350.1:p.Ile443=
ENST00000531303.5:c.*163T=	ENSP00000432625.1:n.*163T=
ENST00000531336.1:n.164T=
ENST00000532367.1:n.168T=
ENST00000533123.5:c.*59T=	ENSP00000435950.1:n.*59T=
ENST00000534405.5:c.*163T=	ENSP00000434353.1:n.*163T=
NM_000543.4:c.1332T=	NP_000534.3:p.Ile444=
NM_001007593.2:c.1329T=	NP_001007594.2:p.Ile443=
XM_005253075.3:c.1332T=	XP_005253132.1:p.Ile444=
XM_011520303.1:c.1200T=	XP_011518605.1:p.Ile400=
XM_011520304.1:c.1200T=	XP_011518606.1:p.Ile400=
XR_930886.1:n.1670T=
NM_001318087.1:c.1332T=	NP_001305016.1:p.Ile444=
NM_001318088.1:c.411T=	NP_001305017.1:p.Ile137=
NM_001365135.1:c.1200T=	NP_001352064.1:p.Ile400=
NR_027400.2:n.1345T=
NR_134502.1:n.864T=
XM_011520304.2:c.1200T=	XP_011518606.1:p.Ile400=
XR_001747940.2:n.1497T=
XR_002957158.1:n.1497T=
NM_000543.5:c.1332T= MANE Select	NP_000534.3:p.Ile444=
NM_001007593.3:c.1329T=	NP_001007594.2:p.Ile443=
NM_001318087.2:c.1332T=	NP_001305016.1:p.Ile444=
NM_001318088.2:c.411T=	NP_001305017.1:p.Ile137=
NM_001365135.2:c.1200T=	NP_001352064.1:p.Ile400=
NR_027400.3:n.1285T=
NR_134502.2:n.804T=