Canonical Allele Identifier: CA1950150289

Gene: SMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394640A= , CM000673.2:g.6394640A=	GRCh38
NC_000011.9:g.6415870A= , CM000673.1:g.6415870A=	GRCh37
NC_000011.8:g.6372446A=	NCBI36
NG_011780.1:g.9216A=
NG_029615.1:g.29775T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*33A= MANE Select	ENSP00000340409.4:n.*33A=
ENST00000342245.8:c.*33A=	ENSP00000340409.4:n.*33A=
ENST00000526280.1:c.986A=
ENST00000527275.5:c.*33A=	ENSP00000435350.1:n.*33A=
ENST00000531303.5:c.*780A=	ENSP00000432625.1:n.*780A=
ENST00000533123.5:c.*656A=	ENSP00000435950.1:n.*656A=
ENST00000534405.5:c.*760A=	ENSP00000434353.1:n.*760A=
NM_000543.4:c.*33A=	NP_000534.3:n.*33A=
NM_001007593.2:c.*33A=	NP_001007594.2:n.*33A=
XM_011520303.1:c.*33A=	XP_011518605.1:n.*33A=
NM_001318087.1:c.*422A=	NP_001305016.1:n.*422A=
NM_001318088.1:c.*33A=	NP_001305017.1:n.*33A=
NM_001365135.1:c.*33A=	NP_001352064.1:n.*33A=
NR_027400.2:n.1942A=
NR_134502.1:n.1481A=
XR_001747940.2:n.2114A=
XR_002957158.1:n.2296A=
NM_000543.5:c.*33A= MANE Select	NP_000534.3:n.*33A=
NM_001007593.3:c.*33A=	NP_001007594.2:n.*33A=
NM_001318087.2:c.*422A=	NP_001305016.1:n.*422A=
NM_001318088.2:c.*33A=	NP_001305017.1:n.*33A=
NM_001365135.2:c.*33A=	NP_001352064.1:n.*33A=
NR_027400.3:n.1882A=
NR_134502.2:n.1421A=