Canonical Allele Identifier: CA2790302103
Gene: SMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390722_6390724del , CM000673.2:g.6390722_6390724del GRCh38
NC_000011.9:g.6411952_6411954del , CM000673.1:g.6411952_6411954del GRCh37
NC_000011.8:g.6368528_6368530del NCBI36
NG_011780.1:g.5298_5300del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.124_126del MANE Select ENSP00000340409.4:p.Ala42del
ENST00000342245.8:c.124_126del ENSP00000340409.4:p.Ala42del
ENST00000527275.5:c.124_126del ENSP00000435350.1:p.Ala42del
ENST00000530395.1:c.-96+83_-96+85del ENSP00000431479.1:n.-96+83_-96+85del
ENST00000531303.5:c.124_126del ENSP00000432625.1:p.Ala42del
ENST00000533123.5:c.124_126del ENSP00000435950.1:p.Ala42del
ENST00000533196.1:n.283_285del
ENST00000534405.5:c.124_126del ENSP00000434353.1:p.Ala42del
NM_000543.4:c.124_126del NP_000534.3:p.Ala42del
NM_001007593.2:c.124_126del NP_001007594.2:p.Ala42del
XM_005253075.3:c.124_126del XP_005253132.1:p.Ala42del
XM_011520303.1:c.124_126del XP_011518605.1:p.Ala42del
XM_011520304.1:c.124_126del XP_011518606.1:p.Ala42del
XR_930886.1:n.422_424del
NM_001318087.1:c.124_126del NP_001305016.1:p.Ala42del
NM_001318088.1:c.-838_-836del NP_001305017.1:n.-838_-836del
NM_001365135.1:c.124_126del NP_001352064.1:p.Ala42del
NR_027400.2:n.309_311del
NR_134502.1:n.309_311del
XM_011520304.2:c.124_126del XP_011518606.1:p.Ala42del
XR_001747940.2:n.249_251del
XR_002957158.1:n.249_251del
NM_000543.5:c.124_126del MANE Select NP_000534.3:p.Ala42del
NM_001007593.3:c.124_126del NP_001007594.2:p.Ala42del
NM_001318087.2:c.124_126del NP_001305016.1:p.Ala42del
NM_001318088.2:c.-838_-836del NP_001305017.1:n.-838_-836del
NM_001365135.2:c.124_126del NP_001352064.1:p.Ala42del
NR_027400.3:n.249_251del
NR_134502.2:n.249_251del