Canonical Allele Identifier: CA373799022
Gene: SPTLC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92068088C>G , CM000671.2:g.92068088C>G GRCh38
NC_000009.11:g.94830370C>G , CM000671.1:g.94830370C>G GRCh37
NC_000009.10:g.93870191C>G NCBI36
NG_007950.1:g.52321G>C , LRG_272:g.52321G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000482632.6:n.848G>C
ENST00000686600.1:c.438G>C ENSP00000509268.1:p.Leu146Phe
ENST00000686799.1:n.535G>C
ENST00000687427.1:c.438G>C ENSP00000509426.1:p.Leu146Phe
ENST00000687817.1:c.*241G>C ENSP00000508926.1:n.*241G>C
ENST00000687972.1:c.498G>C ENSP00000509208.1:p.Leu166Phe
ENST00000689261.1:n.345G>C
ENST00000689401.1:c.*688G>C ENSP00000510251.1:n.*688G>C
ENST00000689423.1:c.*688G>C ENSP00000508519.1:n.*688G>C
ENST00000690095.1:n.766G>C
ENST00000690139.1:c.*139G>C ENSP00000510483.1:n.*139G>C
ENST00000692458.1:n.461G>C
ENST00000693147.1:c.*454G>C ENSP00000510358.1:n.*454G>C
ENST00000262554.7:c.438G>C MANE Select ENSP00000262554.2:p.Leu146Phe
ENST00000642671.1:c.483G>C ENSP00000495764.1:n.483G>C
ENST00000643599.1:c.310G>C ENSP00000494770.1:n.310G>C
ENST00000644140.1:c.*179G>C ENSP00000493933.1:n.*179G>C
ENST00000646481.1:c.310G>C ENSP00000496627.1:n.310G>C
ENST00000646534.1:c.*241G>C ENSP00000495388.1:n.*241G>C
ENST00000262554.6:c.438G>C ENSP00000262554.2:p.Leu146Phe
ENST00000482632.5:n.585G>C
NM_001281303.1:c.438G>C NP_001268232.1:p.Leu146Phe
NM_006415.3:c.438G>C NP_006406.1:p.Leu146Phe
XM_011518138.1:c.438G>C XP_011516440.1:p.Leu146Phe
XM_011518139.1:c.-28G>C XP_011516441.1:n.-28G>C
XM_011518138.2:c.438G>C XP_011516440.1:p.Leu146Phe
XM_011518139.3:c.-28G>C XP_011516441.1:n.-28G>C
XM_017014200.2:c.72G>C XP_016869689.1:p.Leu24Phe
XM_017014201.2:c.72G>C XP_016869690.1:p.Leu24Phe
XM_024447378.1:c.-28G>C XP_024303146.1:n.-28G>C
XM_024447379.1:c.-28G>C XP_024303147.1:n.-28G>C
XR_002956744.1:n.588G>C
NM_006415.4:c.438G>C MANE Select NP_006406.1:p.Leu146Phe
NM_001281303.2:c.438G>C NP_001268232.1:p.Leu146Phe
NM_001368272.1:c.72G>C NP_001355201.1:p.Leu24Phe
NM_001368273.1:c.-28G>C NP_001355202.1:n.-28G>C