Canonical Allele Identifier: CA373795398
Gene: SPTLC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92112480T>A , CM000671.2:g.92112480T>A GRCh38
NC_000009.11:g.94874762T>A , CM000671.1:g.94874762T>A GRCh37
NC_000009.10:g.93914583T>A NCBI36
NG_007950.1:g.7929A>T , LRG_272:g.7929A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000461132.2:c.140A>T ENSP00000509096.1:p.Gln47Leu
ENST00000482632.6:n.550A>T
ENST00000488921.6:c.*156A>T ENSP00000510034.1:n.*156A>T
ENST00000686600.1:c.140A>T ENSP00000509268.1:p.Gln47Leu
ENST00000686799.1:n.237A>T
ENST00000687427.1:c.140A>T ENSP00000509426.1:p.Gln47Leu
ENST00000687817.1:c.140A>T ENSP00000508926.1:p.Gln47Leu
ENST00000687972.1:c.140A>T ENSP00000509208.1:p.Gln47Leu
ENST00000689401.1:c.*156A>T ENSP00000510251.1:n.*156A>T
ENST00000689423.1:c.*156A>T ENSP00000508519.1:n.*156A>T
ENST00000690139.1:c.140A>T ENSP00000510483.1:p.Gln47Leu
ENST00000692363.1:c.140A>T ENSP00000509481.1:p.Gln47Leu
ENST00000692458.1:n.163A>T
ENST00000693147.1:c.*156A>T ENSP00000510358.1:n.*156A>T
ENST00000262554.7:c.140A>T MANE Select ENSP00000262554.2:p.Gln47Leu
ENST00000644140.1:c.140A>T ENSP00000493933.1:p.Gln47Leu
ENST00000646534.1:c.140A>T ENSP00000495388.1:p.Gln47Leu
ENST00000262554.6:c.140A>T ENSP00000262554.2:p.Gln47Leu
ENST00000337841.4:c.140A>T ENSP00000337635.4:p.Gln47Leu
ENST00000461132.1:n.108A>T
ENST00000482632.5:n.154A>T
ENST00000488921.5:n.297A>T
NM_001281303.1:c.140A>T NP_001268232.1:p.Gln47Leu
NM_006415.3:c.140A>T NP_006406.1:p.Gln47Leu
NM_178324.2:c.140A>T NP_847894.1:p.Gln47Leu
XM_011518138.1:c.140A>T XP_011516440.1:p.Gln47Leu
XM_011518139.1:c.-326A>T XP_011516441.1:n.-326A>T
XM_011518138.2:c.140A>T XP_011516440.1:p.Gln47Leu
XM_011518139.3:c.-326A>T XP_011516441.1:n.-326A>T
XM_017014200.2:c.-360A>T XP_016869689.1:n.-360A>T
XM_017014201.2:c.-360A>T XP_016869690.1:n.-360A>T
XR_002956744.1:n.157A>T
NM_006415.4:c.140A>T MANE Select NP_006406.1:p.Gln47Leu
NM_001281303.2:c.140A>T NP_001268232.1:p.Gln47Leu
NM_001368272.1:c.-360A>T NP_001355201.1:n.-360A>T
NM_001368273.1:c.-326A>T NP_001355202.1:n.-326A>T
NM_178324.3:c.140A>T NP_847894.1:p.Gln47Leu