Canonical Allele Identifier: CA373798292

Gene: SPTLC1

Linked Data

• MyVariant Identifiers: chr9:g.94830248A>G (hg19) ; chr9:g.92067966A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92067966A>G , CM000671.2:g.92067966A>G	GRCh38
NC_000009.11:g.94830248A>G , CM000671.1:g.94830248A>G	GRCh37
NC_000009.10:g.93870069A>G	NCBI36
NG_007950.1:g.52443T>C , LRG_272:g.52443T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000482632.6:n.970T>C
ENST00000686600.1:c.560T>C	ENSP00000509268.1:p.Val187Ala
ENST00000686799.1:n.657T>C
ENST00000687427.1:c.560T>C	ENSP00000509426.1:p.Val187Ala
ENST00000687817.1:c.*363T>C	ENSP00000508926.1:n.*363T>C
ENST00000687972.1:c.620T>C	ENSP00000509208.1:p.Val207Ala
ENST00000689261.1:n.467T>C
ENST00000689401.1:c.*810T>C	ENSP00000510251.1:n.*810T>C
ENST00000689423.1:c.*810T>C	ENSP00000508519.1:n.*810T>C
ENST00000690095.1:n.888T>C
ENST00000690139.1:c.*261T>C	ENSP00000510483.1:n.*261T>C
ENST00000692458.1:n.583T>C
ENST00000693147.1:c.*576T>C	ENSP00000510358.1:n.*576T>C
ENST00000262554.7:c.560T>C MANE Select	ENSP00000262554.2:p.Val187Ala
ENST00000642671.1:c.605T>C	ENSP00000495764.1:n.605T>C
ENST00000643599.1:c.432T>C	ENSP00000494770.1:n.432T>C
ENST00000644140.1:c.*301T>C	ENSP00000493933.1:n.*301T>C
ENST00000646481.1:c.432T>C	ENSP00000496627.1:n.432T>C
ENST00000646534.1:c.*363T>C	ENSP00000495388.1:n.*363T>C
ENST00000262554.6:c.560T>C	ENSP00000262554.2:p.Val187Ala
ENST00000482632.5:n.707T>C
NM_001281303.1:c.560T>C	NP_001268232.1:p.Val187Ala
NM_006415.3:c.560T>C	NP_006406.1:p.Val187Ala
XM_011518138.1:c.560T>C	XP_011516440.1:p.Val187Ala
XM_011518139.1:c.95T>C	XP_011516441.1:p.Val32Ala
XM_011518138.2:c.560T>C	XP_011516440.1:p.Val187Ala
XM_011518139.3:c.95T>C	XP_011516441.1:p.Val32Ala
XM_017014200.2:c.194T>C	XP_016869689.1:p.Val65Ala
XM_017014201.2:c.194T>C	XP_016869690.1:p.Val65Ala
XM_024447378.1:c.95T>C	XP_024303146.1:p.Val32Ala
XM_024447379.1:c.95T>C	XP_024303147.1:p.Val32Ala
XR_002956744.1:n.710T>C
NM_006415.4:c.560T>C MANE Select	NP_006406.1:p.Val187Ala
NM_001281303.2:c.560T>C	NP_001268232.1:p.Val187Ala
NM_001368272.1:c.194T>C	NP_001355201.1:p.Val65Ala
NM_001368273.1:c.95T>C	NP_001355202.1:p.Val32Ala