Canonical Allele Identifier: CA379373035
Gene: SMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.6393275T>A , CM000673.2:g.6393275T>A GRCh38
NC_000011.9:g.6414505T>A , CM000673.1:g.6414505T>A GRCh37
NC_000011.8:g.6371081T>A NCBI36
NG_011780.1:g.7851T>A
NG_029615.1:g.31140A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342245.9:c.1151T>A MANE Select ENSP00000340409.4:p.Met384Lys
ENST00000342245.8:c.1151T>A ENSP00000340409.4:p.Met384Lys
ENST00000526280.1:c.321-342T>A
ENST00000527275.5:c.1148T>A ENSP00000435350.1:p.Met383Lys
ENST00000531303.5:c.498T>A ENSP00000432625.1:p.Tyr166Ter
ENST00000533123.5:c.1092-342T>A ENSP00000435950.1:n.1092-342T>A
ENST00000534405.5:c.1191T>A ENSP00000434353.1:p.Tyr397Ter
NM_000543.4:c.1151T>A NP_000534.3:p.Met384Lys
NM_001007593.2:c.1148T>A NP_001007594.2:p.Met383Lys
XM_005253075.3:c.1151T>A XP_005253132.1:p.Met384Lys
XM_011520303.1:c.1132-342T>A XP_011518605.1:n.1132-342T>A
XM_011520304.1:c.1132-342T>A XP_011518606.1:n.1132-342T>A
XR_930886.1:n.1489T>A
NM_001318087.1:c.1151T>A NP_001305016.1:p.Met384Lys
NM_001318088.1:c.230T>A NP_001305017.1:p.Met77Lys
NM_001365135.1:c.1132-342T>A NP_001352064.1:n.1132-342T>A
NR_027400.2:n.1277-342T>A
NR_134502.1:n.683T>A
XM_011520304.2:c.1132-342T>A XP_011518606.1:n.1132-342T>A
XR_001747940.2:n.1316T>A
XR_002957158.1:n.1316T>A
NM_000543.5:c.1151T>A MANE Select NP_000534.3:p.Met384Lys
NM_001007593.3:c.1148T>A NP_001007594.2:p.Met383Lys
NM_001318087.2:c.1151T>A NP_001305016.1:p.Met384Lys
NM_001318088.2:c.230T>A NP_001305017.1:p.Met77Lys
NM_001365135.2:c.1132-342T>A NP_001352064.1:n.1132-342T>A
NR_027400.3:n.1217-342T>A
NR_134502.2:n.623T>A