Canonical Allele Identifier: CA373788965

Gene: SPTLC1

Linked Data

• MyVariant Identifiers: chr9:g.94794778A>C (hg19) ; chr9:g.92032496A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92032496A>C , CM000671.2:g.92032496A>C	GRCh38
NC_000009.11:g.94794778A>C , CM000671.1:g.94794778A>C	GRCh37
NC_000009.10:g.93834599A>C	NCBI36
NG_007950.1:g.87913T>G , LRG_272:g.87913T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686600.1:c.*103T>G	ENSP00000509268.1:n.*103T>G
ENST00000686799.1:n.1715T>G
ENST00000687427.1:c.*147T>G	ENSP00000509426.1:n.*147T>G
ENST00000687817.1:c.*3789T>G	ENSP00000508926.1:n.*3789T>G
ENST00000687972.1:c.1451T>G	ENSP00000509208.1:p.Ile484Ser
ENST00000689261.1:n.1298T>G
ENST00000689401.1:c.*1641T>G	ENSP00000510251.1:n.*1641T>G
ENST00000690095.1:n.1779T>G
ENST00000690139.1:c.*1092T>G	ENSP00000510483.1:n.*1092T>G
ENST00000692458.1:n.2029T>G
ENST00000262554.7:c.1391T>G MANE Select	ENSP00000262554.2:p.Ile464Ser
ENST00000642671.1:c.1629+2314T>G	ENSP00000495764.1:n.1629+2314T>G
ENST00000643599.1:c.1396+2314T>G	ENSP00000494770.1:n.1396+2314T>G
ENST00000644140.1:c.*1132T>G	ENSP00000493933.1:n.*1132T>G
ENST00000646481.1:c.1260+2314T>G	ENSP00000496627.1:n.1260+2314T>G
ENST00000646534.1:c.*1194T>G	ENSP00000495388.1:n.*1194T>G
ENST00000262554.6:c.1391T>G	ENSP00000262554.2:p.Ile464Ser
ENST00000469778.1:n.348T>G
NM_001281303.1:c.1359T>G	NP_001268232.1:p.His453Gln
NM_006415.3:c.1391T>G	NP_006406.1:p.Ile464Ser
XM_011518139.1:c.926T>G	XP_011516441.1:p.Ile309Ser
XM_011518139.3:c.926T>G	XP_011516441.1:p.Ile309Ser
XM_017014200.2:c.1025T>G	XP_016869689.1:p.Ile342Ser
XM_017014201.2:c.1025T>G	XP_016869690.1:p.Ile342Ser
XM_024447378.1:c.926T>G	XP_024303146.1:p.Ile309Ser
XM_024447379.1:c.926T>G	XP_024303147.1:p.Ile309Ser
XR_002956744.1:n.1541T>G
NM_006415.4:c.1391T>G MANE Select	NP_006406.1:p.Ile464Ser
NM_001281303.2:c.1359T>G	NP_001268232.1:p.His453Gln
NM_001368272.1:c.1025T>G	NP_001355201.1:p.Ile342Ser
NM_001368273.1:c.926T>G	NP_001355202.1:p.Ile309Ser