Canonical Allele Identifier: CA373798354

Gene: SPTLC1

Linked Data

• MyVariant Identifiers: chr9:g.94830257A>G (hg19) ; chr9:g.92067975A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92067975A>G , CM000671.2:g.92067975A>G	GRCh38
NC_000009.11:g.94830257A>G , CM000671.1:g.94830257A>G	GRCh37
NC_000009.10:g.93870078A>G	NCBI36
NG_007950.1:g.52434T>C , LRG_272:g.52434T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000482632.6:n.961T>C
ENST00000686600.1:c.551T>C	ENSP00000509268.1:p.Ile184Thr
ENST00000686799.1:n.648T>C
ENST00000687427.1:c.551T>C	ENSP00000509426.1:p.Ile184Thr
ENST00000687817.1:c.*354T>C	ENSP00000508926.1:n.*354T>C
ENST00000687972.1:c.611T>C	ENSP00000509208.1:p.Ile204Thr
ENST00000689261.1:n.458T>C
ENST00000689401.1:c.*801T>C	ENSP00000510251.1:n.*801T>C
ENST00000689423.1:c.*801T>C	ENSP00000508519.1:n.*801T>C
ENST00000690095.1:n.879T>C
ENST00000690139.1:c.*252T>C	ENSP00000510483.1:n.*252T>C
ENST00000692458.1:n.574T>C
ENST00000693147.1:c.*567T>C	ENSP00000510358.1:n.*567T>C
ENST00000262554.7:c.551T>C MANE Select	ENSP00000262554.2:p.Ile184Thr
ENST00000642671.1:c.596T>C	ENSP00000495764.1:n.596T>C
ENST00000643599.1:c.423T>C	ENSP00000494770.1:n.423T>C
ENST00000644140.1:c.*292T>C	ENSP00000493933.1:n.*292T>C
ENST00000646481.1:c.423T>C	ENSP00000496627.1:n.423T>C
ENST00000646534.1:c.*354T>C	ENSP00000495388.1:n.*354T>C
ENST00000262554.6:c.551T>C	ENSP00000262554.2:p.Ile184Thr
ENST00000482632.5:n.698T>C
NM_001281303.1:c.551T>C	NP_001268232.1:p.Ile184Thr
NM_006415.3:c.551T>C	NP_006406.1:p.Ile184Thr
XM_011518138.1:c.551T>C	XP_011516440.1:p.Ile184Thr
XM_011518139.1:c.86T>C	XP_011516441.1:p.Ile29Thr
XM_011518138.2:c.551T>C	XP_011516440.1:p.Ile184Thr
XM_011518139.3:c.86T>C	XP_011516441.1:p.Ile29Thr
XM_017014200.2:c.185T>C	XP_016869689.1:p.Ile62Thr
XM_017014201.2:c.185T>C	XP_016869690.1:p.Ile62Thr
XM_024447378.1:c.86T>C	XP_024303146.1:p.Ile29Thr
XM_024447379.1:c.86T>C	XP_024303147.1:p.Ile29Thr
XR_002956744.1:n.701T>C
NM_006415.4:c.551T>C MANE Select	NP_006406.1:p.Ile184Thr
NM_001281303.2:c.551T>C	NP_001268232.1:p.Ile184Thr
NM_001368272.1:c.185T>C	NP_001355201.1:p.Ile62Thr
NM_001368273.1:c.86T>C	NP_001355202.1:p.Ile29Thr