Canonical Allele Identifier: CA379367161
Gene: SMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390705T>G , CM000673.2:g.6390705T>G GRCh38
NC_000011.9:g.6411935T>G , CM000673.1:g.6411935T>G GRCh37
NC_000011.8:g.6368511T>G NCBI36
NG_011780.1:g.5281T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.107T>G MANE Select ENSP00000340409.4:p.Val36Gly
ENST00000342245.8:c.107T>G ENSP00000340409.4:p.Val36Gly
ENST00000527275.5:c.107T>G ENSP00000435350.1:p.Val36Gly
ENST00000530395.1:c.-96+66T>G ENSP00000431479.1:n.-96+66T>G
ENST00000531303.5:c.107T>G ENSP00000432625.1:p.Val36Gly
ENST00000533123.5:c.107T>G ENSP00000435950.1:p.Val36Gly
ENST00000533196.1:n.266T>G
ENST00000534405.5:c.107T>G ENSP00000434353.1:p.Val36Gly
NM_000543.4:c.107T>G NP_000534.3:p.Val36Gly
NM_001007593.2:c.107T>G NP_001007594.2:p.Val36Gly
XM_005253075.3:c.107T>G XP_005253132.1:p.Val36Gly
XM_011520303.1:c.107T>G XP_011518605.1:p.Val36Gly
XM_011520304.1:c.107T>G XP_011518606.1:p.Val36Gly
XR_930886.1:n.405T>G
NM_001318087.1:c.107T>G NP_001305016.1:p.Val36Gly
NM_001318088.1:c.-855T>G NP_001305017.1:n.-855T>G
NM_001365135.1:c.107T>G NP_001352064.1:p.Val36Gly
NR_027400.2:n.292T>G
NR_134502.1:n.292T>G
XM_011520304.2:c.107T>G XP_011518606.1:p.Val36Gly
XR_001747940.2:n.232T>G
XR_002957158.1:n.232T>G
NM_000543.5:c.107T>G MANE Select NP_000534.3:p.Val36Gly
NM_001007593.3:c.107T>G NP_001007594.2:p.Val36Gly
NM_001318087.2:c.107T>G NP_001305016.1:p.Val36Gly
NM_001318088.2:c.-855T>G NP_001305017.1:n.-855T>G
NM_001365135.2:c.107T>G NP_001352064.1:p.Val36Gly
NR_027400.3:n.232T>G
NR_134502.2:n.232T>G