Canonical Allele Identifier: CA1950147788

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393231T= , CM000673.2:g.6393231T=	GRCh38
NC_000011.9:g.6414461T= , CM000673.1:g.6414461T=	GRCh37
NC_000011.8:g.6371037T=	NCBI36
NG_011780.1:g.7807T=
NG_029615.1:g.31184A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1107T= MANE Select	ENSP00000340409.4:p.Tyr369=
ENST00000342245.8:c.1107T=	ENSP00000340409.4:p.Tyr369=
ENST00000526280.1:c.321-386T=
ENST00000527275.5:c.1104T=	ENSP00000435350.1:p.Tyr368=
ENST00000531303.5:c.454T=	ENSP00000432625.1:p.Cys152=
ENST00000533123.5:c.1092-386T=	ENSP00000435950.1:n.1092-386T=
ENST00000534405.5:c.1147T=	ENSP00000434353.1:p.Cys383=
NM_000543.4:c.1107T=	NP_000534.3:p.Tyr369=
NM_001007593.2:c.1104T=	NP_001007594.2:p.Tyr368=
XM_005253075.3:c.1107T=	XP_005253132.1:p.Tyr369=
XM_011520303.1:c.1132-386T=	XP_011518605.1:n.1132-386T=
XM_011520304.1:c.1132-386T=	XP_011518606.1:n.1132-386T=
XR_930886.1:n.1445T=
NM_001318087.1:c.1107T=	NP_001305016.1:p.Tyr369=
NM_001318088.1:c.186T=	NP_001305017.1:p.Tyr62=
NM_001365135.1:c.1132-386T=	NP_001352064.1:n.1132-386T=
NR_027400.2:n.1277-386T=
NR_134502.1:n.639T=
XM_011520304.2:c.1132-386T=	XP_011518606.1:n.1132-386T=
XR_001747940.2:n.1272T=
XR_002957158.1:n.1272T=
NM_000543.5:c.1107T= MANE Select	NP_000534.3:p.Tyr369=
NM_001007593.3:c.1104T=	NP_001007594.2:p.Tyr368=
NM_001318087.2:c.1107T=	NP_001305016.1:p.Tyr369=
NM_001318088.2:c.186T=	NP_001305017.1:p.Tyr62=
NM_001365135.2:c.1132-386T=	NP_001352064.1:n.1132-386T=
NR_027400.3:n.1217-386T=
NR_134502.2:n.579T=