Canonical Allele Identifier: CA373798319
Gene: SPTLC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92067970A>C , CM000671.2:g.92067970A>C GRCh38
NC_000009.11:g.94830252A>C , CM000671.1:g.94830252A>C GRCh37
NC_000009.10:g.93870073A>C NCBI36
NG_007950.1:g.52439T>G , LRG_272:g.52439T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000482632.6:n.966T>G
ENST00000686600.1:c.556T>G ENSP00000509268.1:p.Phe186Val
ENST00000686799.1:n.653T>G
ENST00000687427.1:c.556T>G ENSP00000509426.1:p.Phe186Val
ENST00000687817.1:c.*359T>G ENSP00000508926.1:n.*359T>G
ENST00000687972.1:c.616T>G ENSP00000509208.1:p.Phe206Val
ENST00000689261.1:n.463T>G
ENST00000689401.1:c.*806T>G ENSP00000510251.1:n.*806T>G
ENST00000689423.1:c.*806T>G ENSP00000508519.1:n.*806T>G
ENST00000690095.1:n.884T>G
ENST00000690139.1:c.*257T>G ENSP00000510483.1:n.*257T>G
ENST00000692458.1:n.579T>G
ENST00000693147.1:c.*572T>G ENSP00000510358.1:n.*572T>G
ENST00000262554.7:c.556T>G MANE Select ENSP00000262554.2:p.Phe186Val
ENST00000642671.1:c.601T>G ENSP00000495764.1:n.601T>G
ENST00000643599.1:c.428T>G ENSP00000494770.1:n.428T>G
ENST00000644140.1:c.*297T>G ENSP00000493933.1:n.*297T>G
ENST00000646481.1:c.428T>G ENSP00000496627.1:n.428T>G
ENST00000646534.1:c.*359T>G ENSP00000495388.1:n.*359T>G
ENST00000262554.6:c.556T>G ENSP00000262554.2:p.Phe186Val
ENST00000482632.5:n.703T>G
NM_001281303.1:c.556T>G NP_001268232.1:p.Phe186Val
NM_006415.3:c.556T>G NP_006406.1:p.Phe186Val
XM_011518138.1:c.556T>G XP_011516440.1:p.Phe186Val
XM_011518139.1:c.91T>G XP_011516441.1:p.Phe31Val
XM_011518138.2:c.556T>G XP_011516440.1:p.Phe186Val
XM_011518139.3:c.91T>G XP_011516441.1:p.Phe31Val
XM_017014200.2:c.190T>G XP_016869689.1:p.Phe64Val
XM_017014201.2:c.190T>G XP_016869690.1:p.Phe64Val
XM_024447378.1:c.91T>G XP_024303146.1:p.Phe31Val
XM_024447379.1:c.91T>G XP_024303147.1:p.Phe31Val
XR_002956744.1:n.706T>G
NM_006415.4:c.556T>G MANE Select NP_006406.1:p.Phe186Val
NM_001281303.2:c.556T>G NP_001268232.1:p.Phe186Val
NM_001368272.1:c.190T>G NP_001355201.1:p.Phe64Val
NM_001368273.1:c.91T>G NP_001355202.1:p.Phe31Val