Canonical Allele Identifier: CA2612223467

Gene: SMPD1

Linked Data

• gnomAD v4: 11-6394126-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6394126G>C , CM000673.2:g.6394126G>C	GRCh38
NC_000011.9:g.6415356G>C , CM000673.1:g.6415356G>C	GRCh37
NC_000011.8:g.6371932G>C	NCBI36
NG_011780.1:g.8702G>C
NG_029615.1:g.30289C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342245.9:c.1487-72G>C MANE Select	ENSP00000340409.4:n.1487-72G>C
ENST00000342245.8:c.1487-72G>C	ENSP00000340409.4:n.1487-72G>C
ENST00000526280.1:c.544-72G>C
ENST00000527275.5:c.1484-72G>C	ENSP00000435350.1:n.1484-72G>C
ENST00000531303.5:c.*318-52G>C	ENSP00000432625.1:n.*318-52G>C
ENST00000531336.1:n.403G>C
ENST00000532367.1:n.407G>C
ENST00000533123.5:c.*214-72G>C	ENSP00000435950.1:n.*214-72G>C
ENST00000534405.5:c.*318-72G>C	ENSP00000434353.1:n.*318-72G>C
NM_000543.4:c.1487-72G>C	NP_000534.3:n.1487-72G>C
NM_001007593.2:c.1484-72G>C	NP_001007594.2:n.1484-72G>C
XM_005253075.3:c.1487-52G>C	XP_005253132.1:n.1487-52G>C
XM_011520303.1:c.1355-72G>C	XP_011518605.1:n.1355-72G>C
XM_011520304.1:c.1355-52G>C	XP_011518606.1:n.1355-52G>C
NM_001318087.1:c.1487-52G>C	NP_001305016.1:n.1487-52G>C
NM_001318088.1:c.566-72G>C	NP_001305017.1:n.566-72G>C
NM_001365135.1:c.1355-72G>C	NP_001352064.1:n.1355-72G>C
NR_027400.2:n.1500-72G>C
NR_134502.1:n.1019-52G>C
XM_011520304.2:c.1355-52G>C	XP_011518606.1:n.1355-52G>C
XR_001747940.2:n.1652-52G>C
XR_002957158.1:n.1854-72G>C
NM_000543.5:c.1487-72G>C MANE Select	NP_000534.3:n.1487-72G>C
NM_001007593.3:c.1484-72G>C	NP_001007594.2:n.1484-72G>C
NM_001318087.2:c.1487-52G>C	NP_001305016.1:n.1487-52G>C
NM_001318088.2:c.566-72G>C	NP_001305017.1:n.566-72G>C
NM_001365135.2:c.1355-72G>C	NP_001352064.1:n.1355-72G>C
NR_027400.3:n.1440-72G>C
NR_134502.2:n.959-52G>C