Canonical Allele Identifier: CA597438130
Gene: SMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1554933850

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6390728_6390745del , CM000673.2:g.6390728_6390745del GRCh38
NC_000011.9:g.6411958_6411975del , CM000673.1:g.6411958_6411975del GRCh37
NC_000011.8:g.6368534_6368551del NCBI36
NG_011780.1:g.5304_5321del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.130_147del MANE Select ENSP00000340409.4:p.Ala44_Leu49del
ENST00000342245.8:c.130_147del ENSP00000340409.4:p.Ala44_Leu49del
ENST00000527275.5:c.130_147del ENSP00000435350.1:p.Ala44_Leu49del
ENST00000530395.1:c.-96+89_-96+106del ENSP00000431479.1:n.-96+89_-96+106del
ENST00000531303.5:c.130_147del ENSP00000432625.1:p.Ala44_Leu49del
ENST00000533123.5:c.130_147del ENSP00000435950.1:p.Ala44_Leu49del
ENST00000533196.1:n.289_306del
ENST00000534405.5:c.130_147del ENSP00000434353.1:p.Ala44_Leu49del
NM_000543.4:c.130_147del NP_000534.3:p.Ala44_Leu49del
NM_001007593.2:c.130_147del NP_001007594.2:p.Ala44_Leu49del
XM_005253075.3:c.130_147del XP_005253132.1:p.Ala44_Leu49del
XM_011520303.1:c.130_147del XP_011518605.1:p.Ala44_Leu49del
XM_011520304.1:c.130_147del XP_011518606.1:p.Ala44_Leu49del
XR_930886.1:n.428_445del
NM_001318087.1:c.130_147del NP_001305016.1:p.Ala44_Leu49del
NM_001318088.1:c.-832_-815del NP_001305017.1:n.-832_-815del
NM_001365135.1:c.130_147del NP_001352064.1:p.Ala44_Leu49del
NR_027400.2:n.315_332del
NR_134502.1:n.315_332del
XM_011520304.2:c.130_147del XP_011518606.1:p.Ala44_Leu49del
XR_001747940.2:n.255_272del
XR_002957158.1:n.255_272del
NM_000543.5:c.130_147del MANE Select NP_000534.3:p.Ala44_Leu49del
NM_001007593.3:c.130_147del NP_001007594.2:p.Ala44_Leu49del
NM_001318087.2:c.130_147del NP_001305016.1:p.Ala44_Leu49del
NM_001318088.2:c.-832_-815del NP_001305017.1:n.-832_-815del
NM_001365135.2:c.130_147del NP_001352064.1:p.Ala44_Leu49del
NR_027400.3:n.255_272del
NR_134502.2:n.255_272del