Canonical Allele Identifier: CA379371055
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1847933499
gnomAD v3: 11-6391876-C-T
gnomAD v4: 11-6391876-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6391876C>T , CM000673.2:g.6391876C>T GRCh38
NC_000011.9:g.6413106C>T , CM000673.1:g.6413106C>T GRCh37
NC_000011.8:g.6369682C>T NCBI36
NG_011780.1:g.6452C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000342245.9:c.811C>T MANE Select ENSP00000340409.4:p.Pro271Ser
ENST00000342245.8:c.811C>T ENSP00000340409.4:p.Pro271Ser
ENST00000527275.5:c.808C>T ENSP00000435350.1:p.Pro270Ser
ENST00000530395.1:c.-9C>T ENSP00000431479.1:n.-9C>T
ENST00000531303.5:c.438+373C>T ENSP00000432625.1:n.438+373C>T
ENST00000533123.5:c.811C>T ENSP00000435950.1:p.Pro271Ser
ENST00000533196.1:n.375-130C>T
ENST00000534405.5:c.811C>T ENSP00000434353.1:p.Pro271Ser
NM_000543.4:c.811C>T NP_000534.3:p.Pro271Ser
NM_001007593.2:c.808C>T NP_001007594.2:p.Pro270Ser
XM_005253075.3:c.811C>T XP_005253132.1:p.Pro271Ser
XM_011520303.1:c.811C>T XP_011518605.1:p.Pro271Ser
XM_011520304.1:c.811C>T XP_011518606.1:p.Pro271Ser
XR_930886.1:n.1109C>T
NM_001318087.1:c.811C>T NP_001305016.1:p.Pro271Ser
NM_001318088.1:c.-151C>T NP_001305017.1:n.-151C>T
NM_001365135.1:c.811C>T NP_001352064.1:p.Pro271Ser
NR_027400.2:n.996C>T
NR_134502.1:n.623+373C>T
XM_011520304.2:c.811C>T XP_011518606.1:p.Pro271Ser
XR_001747940.2:n.936C>T
XR_002957158.1:n.936C>T
NM_000543.5:c.811C>T MANE Select NP_000534.3:p.Pro271Ser
NM_001007593.3:c.808C>T NP_001007594.2:p.Pro270Ser
NM_001318087.2:c.811C>T NP_001305016.1:p.Pro271Ser
NM_001318088.2:c.-151C>T NP_001305017.1:n.-151C>T
NM_001365135.2:c.811C>T NP_001352064.1:p.Pro271Ser
NR_027400.3:n.936C>T
NR_134502.2:n.563+373C>T