Canonical Allele Identifier: CA2612224512

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6394951-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394951T>C , CM000673.2:g.6394951T>C	GRCh38
NC_000011.9:g.6416181T>C , CM000673.1:g.6416181T>C	GRCh37
NC_000011.8:g.6372757T>C	NCBI36
NG_011780.1:g.9527T>C
NG_029615.1:g.29464A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.*344T>C MANE Select	ENSP00000340409.4:n.*344T>C
ENST00000342245.8:c.*344T>C	ENSP00000340409.4:n.*344T>C
ENST00000526280.1:c.1297T>C
ENST00000533123.5:c.*967T>C	ENSP00000435950.1:n.*967T>C
ENST00000534405.5:c.*1071T>C	ENSP00000434353.1:n.*1071T>C
NM_000543.4:c.*344T>C	NP_000534.3:n.*344T>C
NM_001007593.2:c.*344T>C	NP_001007594.2:n.*344T>C
XM_011520303.1:c.*344T>C	XP_011518605.1:n.*344T>C
NM_001318087.1:c.*733T>C	NP_001305016.1:n.*733T>C
NM_001318088.1:c.*344T>C	NP_001305017.1:n.*344T>C
NM_001365135.1:c.*344T>C	NP_001352064.1:n.*344T>C
NR_027400.2:n.2253T>C
NR_134502.1:n.1792T>C
XR_001747940.2:n.2425T>C
XR_002957158.1:n.2607T>C
NM_000543.5:c.*344T>C MANE Select	NP_000534.3:n.*344T>C
NM_001007593.3:c.*344T>C	NP_001007594.2:n.*344T>C
NM_001318087.2:c.*733T>C	NP_001305016.1:n.*733T>C
NM_001318088.2:c.*344T>C	NP_001305017.1:n.*344T>C
NM_001365135.2:c.*344T>C	NP_001352064.1:n.*344T>C
NR_027400.3:n.2193T>C
NR_134502.2:n.1732T>C