Canonical Allele Identifier: CA2612224435

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6394896-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394896C>A , CM000673.2:g.6394896C>A	GRCh38
NC_000011.9:g.6416126C>A , CM000673.1:g.6416126C>A	GRCh37
NC_000011.8:g.6372702C>A	NCBI36
NG_011780.1:g.9472C>A
NG_029615.1:g.29519G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*289C>A MANE Select	ENSP00000340409.4:n.*289C>A
ENST00000342245.8:c.*289C>A	ENSP00000340409.4:n.*289C>A
ENST00000526280.1:c.1242C>A
ENST00000533123.5:c.*912C>A	ENSP00000435950.1:n.*912C>A
ENST00000534405.5:c.*1016C>A	ENSP00000434353.1:n.*1016C>A
NM_000543.4:c.*289C>A	NP_000534.3:n.*289C>A
NM_001007593.2:c.*289C>A	NP_001007594.2:n.*289C>A
XM_011520303.1:c.*289C>A	XP_011518605.1:n.*289C>A
NM_001318087.1:c.*678C>A	NP_001305016.1:n.*678C>A
NM_001318088.1:c.*289C>A	NP_001305017.1:n.*289C>A
NM_001365135.1:c.*289C>A	NP_001352064.1:n.*289C>A
NR_027400.2:n.2198C>A
NR_134502.1:n.1737C>A
XR_001747940.2:n.2370C>A
XR_002957158.1:n.2552C>A
NM_000543.5:c.*289C>A MANE Select	NP_000534.3:n.*289C>A
NM_001007593.3:c.*289C>A	NP_001007594.2:n.*289C>A
NM_001318087.2:c.*678C>A	NP_001305016.1:n.*678C>A
NM_001318088.2:c.*289C>A	NP_001305017.1:n.*289C>A
NM_001365135.2:c.*289C>A	NP_001352064.1:n.*289C>A
NR_027400.3:n.2138C>A
NR_134502.2:n.1677C>A