Canonical Allele Identifier: CA2612223261

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6393588-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6393588T>C , CM000673.2:g.6393588T>C	GRCh38
NC_000011.9:g.6414818T>C , CM000673.1:g.6414818T>C	GRCh37
NC_000011.8:g.6371394T>C	NCBI36
NG_011780.1:g.8164T>C
NG_029615.1:g.30827A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342245.9:c.1264-29T>C MANE Select	ENSP00000340409.4:n.1264-29T>C
ENST00000342245.8:c.1264-29T>C	ENSP00000340409.4:n.1264-29T>C
ENST00000526280.1:c.321-29T>C
ENST00000527275.5:c.1261-29T>C	ENSP00000435350.1:n.1261-29T>C
ENST00000531303.5:c.*95-29T>C	ENSP00000432625.1:n.*95-29T>C
ENST00000531336.1:n.96-29T>C
ENST00000532367.1:n.71T>C
ENST00000533123.5:c.1092-29T>C	ENSP00000435950.1:n.1092-29T>C
ENST00000534405.5:c.*95-29T>C	ENSP00000434353.1:n.*95-29T>C
NM_000543.4:c.1264-29T>C	NP_000534.3:n.1264-29T>C
NM_001007593.2:c.1261-29T>C	NP_001007594.2:n.1261-29T>C
XM_005253075.3:c.1264-29T>C	XP_005253132.1:n.1264-29T>C
XM_011520303.1:c.1132-29T>C	XP_011518605.1:n.1132-29T>C
XM_011520304.1:c.1132-29T>C	XP_011518606.1:n.1132-29T>C
XR_930886.1:n.1602-29T>C
NM_001318087.1:c.1264-29T>C	NP_001305016.1:n.1264-29T>C
NM_001318088.1:c.343-29T>C	NP_001305017.1:n.343-29T>C
NM_001365135.1:c.1132-29T>C	NP_001352064.1:n.1132-29T>C
NR_027400.2:n.1277-29T>C
NR_134502.1:n.796-29T>C
XM_011520304.2:c.1132-29T>C	XP_011518606.1:n.1132-29T>C
XR_001747940.2:n.1429-29T>C
XR_002957158.1:n.1429-29T>C
NM_000543.5:c.1264-29T>C MANE Select	NP_000534.3:n.1264-29T>C
NM_001007593.3:c.1261-29T>C	NP_001007594.2:n.1261-29T>C
NM_001318087.2:c.1264-29T>C	NP_001305016.1:n.1264-29T>C
NM_001318088.2:c.343-29T>C	NP_001305017.1:n.343-29T>C
NM_001365135.2:c.1132-29T>C	NP_001352064.1:n.1132-29T>C
NR_027400.3:n.1217-29T>C
NR_134502.2:n.736-29T>C