Canonical Allele Identifier: CA373789011

Gene: SPTLC1

Linked Data

• MyVariant Identifiers: chr9:g.94794785A>T (hg19) ; chr9:g.92032503A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92032503A>T , CM000671.2:g.92032503A>T	GRCh38
NC_000009.11:g.94794785A>T , CM000671.1:g.94794785A>T	GRCh37
NC_000009.10:g.93834606A>T	NCBI36
NG_007950.1:g.87906T>A , LRG_272:g.87906T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686600.1:c.*96T>A	ENSP00000509268.1:n.*96T>A
ENST00000686799.1:n.1708T>A
ENST00000687427.1:c.*140T>A	ENSP00000509426.1:n.*140T>A
ENST00000687817.1:c.*3782T>A	ENSP00000508926.1:n.*3782T>A
ENST00000687972.1:c.1444T>A	ENSP00000509208.1:p.Ser482Thr
ENST00000689261.1:n.1291T>A
ENST00000689401.1:c.*1634T>A	ENSP00000510251.1:n.*1634T>A
ENST00000690095.1:n.1772T>A
ENST00000690139.1:c.*1085T>A	ENSP00000510483.1:n.*1085T>A
ENST00000692458.1:n.2022T>A
ENST00000262554.7:c.1384T>A MANE Select	ENSP00000262554.2:p.Ser462Thr
ENST00000642671.1:c.1629+2307T>A	ENSP00000495764.1:n.1629+2307T>A
ENST00000643599.1:c.1396+2307T>A	ENSP00000494770.1:n.1396+2307T>A
ENST00000644140.1:c.*1125T>A	ENSP00000493933.1:n.*1125T>A
ENST00000646481.1:c.1260+2307T>A	ENSP00000496627.1:n.1260+2307T>A
ENST00000646534.1:c.*1187T>A	ENSP00000495388.1:n.*1187T>A
ENST00000262554.6:c.1384T>A	ENSP00000262554.2:p.Ser462Thr
ENST00000469778.1:n.341T>A
NM_001281303.1:c.1352T>A	NP_001268232.1:p.Val451Asp
NM_006415.3:c.1384T>A	NP_006406.1:p.Ser462Thr
XM_011518139.1:c.919T>A	XP_011516441.1:p.Ser307Thr
XM_011518139.3:c.919T>A	XP_011516441.1:p.Ser307Thr
XM_017014200.2:c.1018T>A	XP_016869689.1:p.Ser340Thr
XM_017014201.2:c.1018T>A	XP_016869690.1:p.Ser340Thr
XM_024447378.1:c.919T>A	XP_024303146.1:p.Ser307Thr
XM_024447379.1:c.919T>A	XP_024303147.1:p.Ser307Thr
XR_002956744.1:n.1534T>A
NM_006415.4:c.1384T>A MANE Select	NP_006406.1:p.Ser462Thr
NM_001281303.2:c.1352T>A	NP_001268232.1:p.Val451Asp
NM_001368272.1:c.1018T>A	NP_001355201.1:p.Ser340Thr
NM_001368273.1:c.919T>A	NP_001355202.1:p.Ser307Thr