Canonical Allele Identifier: CA2790301988
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390520C>T , CM000673.2:g.6390520C>T GRCh38
NC_000011.9:g.6411750C>T , CM000673.1:g.6411750C>T GRCh37
NC_000011.8:g.6368326C>T NCBI36
NG_011780.1:g.5096C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.-79C>T MANE Select ENSP00000340409.4:n.-79C>T
ENST00000342245.8:c.-79C>T ENSP00000340409.4:n.-79C>T
ENST00000527275.5:c.-79C>T ENSP00000435350.1:n.-79C>T
ENST00000530395.1:c.-215C>T ENSP00000431479.1:n.-215C>T
ENST00000533123.5:c.-79C>T ENSP00000435950.1:n.-79C>T
ENST00000533196.1:n.81C>T
ENST00000534405.5:c.-79C>T ENSP00000434353.1:n.-79C>T
NM_000543.4:c.-79C>T NP_000534.3:n.-79C>T
NM_001007593.2:c.-79C>T NP_001007594.2:n.-79C>T
XM_005253075.3:c.-79C>T XP_005253132.1:n.-79C>T
XM_011520303.1:c.-79C>T XP_011518605.1:n.-79C>T
XM_011520304.1:c.-79C>T XP_011518606.1:n.-79C>T
XR_930886.1:n.220C>T
NM_001318087.1:c.-79C>T NP_001305016.1:n.-79C>T
NM_001318088.1:c.-1040C>T NP_001305017.1:n.-1040C>T
NM_001365135.1:c.-79C>T NP_001352064.1:n.-79C>T
NR_027400.2:n.107C>T
NR_134502.1:n.107C>T
XM_011520304.2:c.-79C>T XP_011518606.1:n.-79C>T
XR_001747940.2:n.47C>T
XR_002957158.1:n.47C>T
NM_000543.5:c.-79C>T MANE Select NP_000534.3:n.-79C>T
NM_001007593.3:c.-79C>T NP_001007594.2:n.-79C>T
NM_001318087.2:c.-79C>T NP_001305016.1:n.-79C>T
NM_001318088.2:c.-1040C>T NP_001305017.1:n.-1040C>T
NM_001365135.2:c.-79C>T NP_001352064.1:n.-79C>T
NR_027400.3:n.47C>T
NR_134502.2:n.47C>T