Canonical Allele Identifier: CA1950145565
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1564921162

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390522G>A , CM000673.2:g.6390522G>A GRCh38
NC_000011.9:g.6411752G>A , CM000673.1:g.6411752G>A GRCh37
NC_000011.8:g.6368328G>A NCBI36
NG_011780.1:g.5098G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.-77G>A MANE Select ENSP00000340409.4:n.-77G>A
ENST00000342245.8:c.-77G>A ENSP00000340409.4:n.-77G>A
ENST00000527275.5:c.-77G>A ENSP00000435350.1:n.-77G>A
ENST00000530395.1:c.-213G>A ENSP00000431479.1:n.-213G>A
ENST00000533123.5:c.-77G>A ENSP00000435950.1:n.-77G>A
ENST00000533196.1:n.83G>A
ENST00000534405.5:c.-77G>A ENSP00000434353.1:n.-77G>A
NM_000543.4:c.-77G>A NP_000534.3:n.-77G>A
NM_001007593.2:c.-77G>A NP_001007594.2:n.-77G>A
XM_005253075.3:c.-77G>A XP_005253132.1:n.-77G>A
XM_011520303.1:c.-77G>A XP_011518605.1:n.-77G>A
XM_011520304.1:c.-77G>A XP_011518606.1:n.-77G>A
XR_930886.1:n.222G>A
NM_001318087.1:c.-77G>A NP_001305016.1:n.-77G>A
NM_001318088.1:c.-1038G>A NP_001305017.1:n.-1038G>A
NM_001365135.1:c.-77G>A NP_001352064.1:n.-77G>A
NR_027400.2:n.109G>A
NR_134502.1:n.109G>A
XM_011520304.2:c.-77G>A XP_011518606.1:n.-77G>A
XR_001747940.2:n.49G>A
XR_002957158.1:n.49G>A
NM_000543.5:c.-77G>A MANE Select NP_000534.3:n.-77G>A
NM_001007593.3:c.-77G>A NP_001007594.2:n.-77G>A
NM_001318087.2:c.-77G>A NP_001305016.1:n.-77G>A
NM_001318088.2:c.-1038G>A NP_001305017.1:n.-1038G>A
NM_001365135.2:c.-77G>A NP_001352064.1:n.-77G>A
NR_027400.3:n.49G>A
NR_134502.2:n.49G>A