Canonical Allele Identifier: CA465998656

Gene: SPTLC1

Linked Data

• MyVariant Identifiers: chr9:g.94830298G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92068016G>T , CM000671.2:g.92068016G>T	GRCh38
NC_000009.11:g.94830298G>T , CM000671.1:g.94830298G>T	GRCh37
NC_000009.10:g.93870119G>T	NCBI36
NG_007950.1:g.52393C>A , LRG_272:g.52393C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482632.6:n.920C>A
ENST00000686600.1:c.510C>A	ENSP00000509268.1:p.Thr170=
ENST00000686799.1:n.607C>A
ENST00000687427.1:c.510C>A	ENSP00000509426.1:p.Thr170=
ENST00000687817.1:c.*313C>A	ENSP00000508926.1:n.*313C>A
ENST00000687972.1:c.570C>A	ENSP00000509208.1:p.Thr190=
ENST00000689261.1:n.417C>A
ENST00000689401.1:c.*760C>A	ENSP00000510251.1:n.*760C>A
ENST00000689423.1:c.*760C>A	ENSP00000508519.1:n.*760C>A
ENST00000690095.1:n.838C>A
ENST00000690139.1:c.*211C>A	ENSP00000510483.1:n.*211C>A
ENST00000692458.1:n.533C>A
ENST00000693147.1:c.*526C>A	ENSP00000510358.1:n.*526C>A
ENST00000262554.7:c.510C>A MANE Select	ENSP00000262554.2:p.Thr170=
ENST00000642671.1:c.555C>A	ENSP00000495764.1:n.555C>A
ENST00000643599.1:c.382C>A	ENSP00000494770.1:n.382C>A
ENST00000644140.1:c.*251C>A	ENSP00000493933.1:n.*251C>A
ENST00000646481.1:c.382C>A	ENSP00000496627.1:n.382C>A
ENST00000646534.1:c.*313C>A	ENSP00000495388.1:n.*313C>A
ENST00000262554.6:c.510C>A	ENSP00000262554.2:p.Thr170=
ENST00000482632.5:n.657C>A
NM_001281303.1:c.510C>A	NP_001268232.1:p.Thr170=
NM_006415.3:c.510C>A	NP_006406.1:p.Thr170=
XM_011518138.1:c.510C>A	XP_011516440.1:p.Thr170=
XM_011518139.1:c.45C>A	XP_011516441.1:p.Thr15=
XM_011518138.2:c.510C>A	XP_011516440.1:p.Thr170=
XM_011518139.3:c.45C>A	XP_011516441.1:p.Thr15=
XM_017014200.2:c.144C>A	XP_016869689.1:p.Thr48=
XM_017014201.2:c.144C>A	XP_016869690.1:p.Thr48=
XM_024447378.1:c.45C>A	XP_024303146.1:p.Thr15=
XM_024447379.1:c.45C>A	XP_024303147.1:p.Thr15=
XR_002956744.1:n.660C>A
NM_006415.4:c.510C>A MANE Select	NP_006406.1:p.Thr170=
NM_001281303.2:c.510C>A	NP_001268232.1:p.Thr170=
NM_001368272.1:c.144C>A	NP_001355201.1:p.Thr48=
NM_001368273.1:c.45C>A	NP_001355202.1:p.Thr15=