Canonical Allele Identifier: CA217301908
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1022156039

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6393573G>A , CM000673.2:g.6393573G>A GRCh38
NC_000011.9:g.6414803G>A , CM000673.1:g.6414803G>A GRCh37
NC_000011.8:g.6371379G>A NCBI36
NG_011780.1:g.8149G>A
NG_029615.1:g.30842C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.1264-44G>A MANE Select ENSP00000340409.4:n.1264-44G>A
ENST00000342245.8:c.1264-44G>A ENSP00000340409.4:n.1264-44G>A
ENST00000526280.1:c.321-44G>A
ENST00000527275.5:c.1261-44G>A ENSP00000435350.1:n.1261-44G>A
ENST00000531303.5:c.*95-44G>A ENSP00000432625.1:n.*95-44G>A
ENST00000531336.1:n.96-44G>A
ENST00000532367.1:n.56G>A
ENST00000533123.5:c.1092-44G>A ENSP00000435950.1:n.1092-44G>A
ENST00000534405.5:c.*95-44G>A ENSP00000434353.1:n.*95-44G>A
NM_000543.4:c.1264-44G>A NP_000534.3:n.1264-44G>A
NM_001007593.2:c.1261-44G>A NP_001007594.2:n.1261-44G>A
XM_005253075.3:c.1264-44G>A XP_005253132.1:n.1264-44G>A
XM_011520303.1:c.1132-44G>A XP_011518605.1:n.1132-44G>A
XM_011520304.1:c.1132-44G>A XP_011518606.1:n.1132-44G>A
XR_930886.1:n.1602-44G>A
NM_001318087.1:c.1264-44G>A NP_001305016.1:n.1264-44G>A
NM_001318088.1:c.343-44G>A NP_001305017.1:n.343-44G>A
NM_001365135.1:c.1132-44G>A NP_001352064.1:n.1132-44G>A
NR_027400.2:n.1277-44G>A
NR_134502.1:n.796-44G>A
XM_011520304.2:c.1132-44G>A XP_011518606.1:n.1132-44G>A
XR_001747940.2:n.1429-44G>A
XR_002957158.1:n.1429-44G>A
NM_000543.5:c.1264-44G>A MANE Select NP_000534.3:n.1264-44G>A
NM_001007593.3:c.1261-44G>A NP_001007594.2:n.1261-44G>A
NM_001318087.2:c.1264-44G>A NP_001305016.1:n.1264-44G>A
NM_001318088.2:c.343-44G>A NP_001305017.1:n.343-44G>A
NM_001365135.2:c.1132-44G>A NP_001352064.1:n.1132-44G>A
NR_027400.3:n.1217-44G>A
NR_134502.2:n.736-44G>A