Canonical Allele Identifier: CA1950150427

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394779A= , CM000673.2:g.6394779A=	GRCh38
NC_000011.9:g.6416009A= , CM000673.1:g.6416009A=	GRCh37
NC_000011.8:g.6372585A=	NCBI36
NG_011780.1:g.9355A=
NG_029615.1:g.29636T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*172A= MANE Select	ENSP00000340409.4:n.*172A=
ENST00000342245.8:c.*172A=	ENSP00000340409.4:n.*172A=
ENST00000526280.1:c.1125A=
ENST00000533123.5:c.*795A=	ENSP00000435950.1:n.*795A=
ENST00000534405.5:c.*899A=	ENSP00000434353.1:n.*899A=
NM_000543.4:c.*172A=	NP_000534.3:n.*172A=
NM_001007593.2:c.*172A=	NP_001007594.2:n.*172A=
XM_011520303.1:c.*172A=	XP_011518605.1:n.*172A=
NM_001318087.1:c.*561A=	NP_001305016.1:n.*561A=
NM_001318088.1:c.*172A=	NP_001305017.1:n.*172A=
NM_001365135.1:c.*172A=	NP_001352064.1:n.*172A=
NR_027400.2:n.2081A=
NR_134502.1:n.1620A=
XR_001747940.2:n.2253A=
XR_002957158.1:n.2435A=
NM_000543.5:c.*172A= MANE Select	NP_000534.3:n.*172A=
NM_001007593.3:c.*172A=	NP_001007594.2:n.*172A=
NM_001318087.2:c.*561A=	NP_001305016.1:n.*561A=
NM_001318088.2:c.*172A=	NP_001305017.1:n.*172A=
NM_001365135.2:c.*172A=	NP_001352064.1:n.*172A=
NR_027400.3:n.2021A=
NR_134502.2:n.1560A=