Canonical Allele Identifier: CA2612224192

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6394697-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394697C>T , CM000673.2:g.6394697C>T	GRCh38
NC_000011.9:g.6415927C>T , CM000673.1:g.6415927C>T	GRCh37
NC_000011.8:g.6372503C>T	NCBI36
NG_011780.1:g.9273C>T
NG_029615.1:g.29718G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*90C>T MANE Select	ENSP00000340409.4:n.*90C>T
ENST00000342245.8:c.*90C>T	ENSP00000340409.4:n.*90C>T
ENST00000526280.1:c.1043C>T
ENST00000527275.5:c.*90C>T	ENSP00000435350.1:n.*90C>T
ENST00000531303.5:c.*837C>T	ENSP00000432625.1:n.*837C>T
ENST00000533123.5:c.*713C>T	ENSP00000435950.1:n.*713C>T
ENST00000534405.5:c.*817C>T	ENSP00000434353.1:n.*817C>T
NM_000543.4:c.*90C>T	NP_000534.3:n.*90C>T
NM_001007593.2:c.*90C>T	NP_001007594.2:n.*90C>T
XM_011520303.1:c.*90C>T	XP_011518605.1:n.*90C>T
NM_001318087.1:c.*479C>T	NP_001305016.1:n.*479C>T
NM_001318088.1:c.*90C>T	NP_001305017.1:n.*90C>T
NM_001365135.1:c.*90C>T	NP_001352064.1:n.*90C>T
NR_027400.2:n.1999C>T
NR_134502.1:n.1538C>T
XR_001747940.2:n.2171C>T
XR_002957158.1:n.2353C>T
NM_000543.5:c.*90C>T MANE Select	NP_000534.3:n.*90C>T
NM_001007593.3:c.*90C>T	NP_001007594.2:n.*90C>T
NM_001318087.2:c.*479C>T	NP_001305016.1:n.*479C>T
NM_001318088.2:c.*90C>T	NP_001305017.1:n.*90C>T
NM_001365135.2:c.*90C>T	NP_001352064.1:n.*90C>T
NR_027400.3:n.1939C>T
NR_134502.2:n.1478C>T