Canonical Allele Identifier: CA465998451

Gene: SPTLC1

Linked Data

• MyVariant Identifiers: chr9:g.94830265T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92067983T>C , CM000671.2:g.92067983T>C	GRCh38
NC_000009.11:g.94830265T>C , CM000671.1:g.94830265T>C	GRCh37
NC_000009.10:g.93870086T>C	NCBI36
NG_007950.1:g.52426A>G , LRG_272:g.52426A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482632.6:n.953A>G
ENST00000686600.1:c.543A>G	ENSP00000509268.1:p.Arg181=
ENST00000686799.1:n.640A>G
ENST00000687427.1:c.543A>G	ENSP00000509426.1:p.Arg181=
ENST00000687817.1:c.*346A>G	ENSP00000508926.1:n.*346A>G
ENST00000687972.1:c.603A>G	ENSP00000509208.1:p.Arg201=
ENST00000689261.1:n.450A>G
ENST00000689401.1:c.*793A>G	ENSP00000510251.1:n.*793A>G
ENST00000689423.1:c.*793A>G	ENSP00000508519.1:n.*793A>G
ENST00000690095.1:n.871A>G
ENST00000690139.1:c.*244A>G	ENSP00000510483.1:n.*244A>G
ENST00000692458.1:n.566A>G
ENST00000693147.1:c.*559A>G	ENSP00000510358.1:n.*559A>G
ENST00000262554.7:c.543A>G MANE Select	ENSP00000262554.2:p.Arg181=
ENST00000642671.1:c.588A>G	ENSP00000495764.1:n.588A>G
ENST00000643599.1:c.415A>G	ENSP00000494770.1:n.415A>G
ENST00000644140.1:c.*284A>G	ENSP00000493933.1:n.*284A>G
ENST00000646481.1:c.415A>G	ENSP00000496627.1:n.415A>G
ENST00000646534.1:c.*346A>G	ENSP00000495388.1:n.*346A>G
ENST00000262554.6:c.543A>G	ENSP00000262554.2:p.Arg181=
ENST00000482632.5:n.690A>G
NM_001281303.1:c.543A>G	NP_001268232.1:p.Arg181=
NM_006415.3:c.543A>G	NP_006406.1:p.Arg181=
XM_011518138.1:c.543A>G	XP_011516440.1:p.Arg181=
XM_011518139.1:c.78A>G	XP_011516441.1:p.Arg26=
XM_011518138.2:c.543A>G	XP_011516440.1:p.Arg181=
XM_011518139.3:c.78A>G	XP_011516441.1:p.Arg26=
XM_017014200.2:c.177A>G	XP_016869689.1:p.Arg59=
XM_017014201.2:c.177A>G	XP_016869690.1:p.Arg59=
XM_024447378.1:c.78A>G	XP_024303146.1:p.Arg26=
XM_024447379.1:c.78A>G	XP_024303147.1:p.Arg26=
XR_002956744.1:n.693A>G
NM_006415.4:c.543A>G MANE Select	NP_006406.1:p.Arg181=
NM_001281303.2:c.543A>G	NP_001268232.1:p.Arg181=
NM_001368272.1:c.177A>G	NP_001355201.1:p.Arg59=
NM_001368273.1:c.78A>G	NP_001355202.1:p.Arg26=