Canonical Allele Identifier: CA1950150578

Gene: SMPD1

Linked Data

• dbSNP Id: rs1848123574
• gnomAD v4: 11-6394941-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394941T>C , CM000673.2:g.6394941T>C	GRCh38
NC_000011.9:g.6416171T>C , CM000673.1:g.6416171T>C	GRCh37
NC_000011.8:g.6372747T>C	NCBI36
NG_011780.1:g.9517T>C
NG_029615.1:g.29474A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*334T>C MANE Select	ENSP00000340409.4:n.*334T>C
ENST00000342245.8:c.*334T>C	ENSP00000340409.4:n.*334T>C
ENST00000526280.1:c.1287T>C
ENST00000533123.5:c.*957T>C	ENSP00000435950.1:n.*957T>C
ENST00000534405.5:c.*1061T>C	ENSP00000434353.1:n.*1061T>C
NM_000543.4:c.*334T>C	NP_000534.3:n.*334T>C
NM_001007593.2:c.*334T>C	NP_001007594.2:n.*334T>C
XM_011520303.1:c.*334T>C	XP_011518605.1:n.*334T>C
NM_001318087.1:c.*723T>C	NP_001305016.1:n.*723T>C
NM_001318088.1:c.*334T>C	NP_001305017.1:n.*334T>C
NM_001365135.1:c.*334T>C	NP_001352064.1:n.*334T>C
NR_027400.2:n.2243T>C
NR_134502.1:n.1782T>C
XR_001747940.2:n.2415T>C
XR_002957158.1:n.2597T>C
NM_000543.5:c.*334T>C MANE Select	NP_000534.3:n.*334T>C
NM_001007593.3:c.*334T>C	NP_001007594.2:n.*334T>C
NM_001318087.2:c.*723T>C	NP_001305016.1:n.*723T>C
NM_001318088.2:c.*334T>C	NP_001305017.1:n.*334T>C
NM_001365135.2:c.*334T>C	NP_001352064.1:n.*334T>C
NR_027400.3:n.2183T>C
NR_134502.2:n.1722T>C