Canonical Allele Identifier: CA1864081059

Gene: SPTLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92068049T= , CM000671.2:g.92068049T=	GRCh38
NC_000009.11:g.94830331T= , CM000671.1:g.94830331T=	GRCh37
NC_000009.10:g.93870152T=	NCBI36
NG_007950.1:g.52360A= , LRG_272:g.52360A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482632.6:n.887A=
ENST00000686600.1:c.477A=	ENSP00000509268.1:p.Glu159=
ENST00000686799.1:n.574A=
ENST00000687427.1:c.477A=	ENSP00000509426.1:p.Glu159=
ENST00000687817.1:c.*280A=	ENSP00000508926.1:n.*280A=
ENST00000687972.1:c.537A=	ENSP00000509208.1:p.Glu179=
ENST00000689261.1:n.384A=
ENST00000689401.1:c.*727A=	ENSP00000510251.1:n.*727A=
ENST00000689423.1:c.*727A=	ENSP00000508519.1:n.*727A=
ENST00000690095.1:n.805A=
ENST00000690139.1:c.*178A=	ENSP00000510483.1:n.*178A=
ENST00000692458.1:n.500A=
ENST00000693147.1:c.*493A=	ENSP00000510358.1:n.*493A=
ENST00000262554.7:c.477A= MANE Select	ENSP00000262554.2:p.Glu159=
ENST00000642671.1:c.522A=	ENSP00000495764.1:n.522A=
ENST00000643599.1:c.349A=	ENSP00000494770.1:n.349A=
ENST00000644140.1:c.*218A=	ENSP00000493933.1:n.*218A=
ENST00000646481.1:c.349A=	ENSP00000496627.1:n.349A=
ENST00000646534.1:c.*280A=	ENSP00000495388.1:n.*280A=
ENST00000262554.6:c.477A=	ENSP00000262554.2:p.Glu159=
ENST00000482632.5:n.624A=
NM_001281303.1:c.477A=	NP_001268232.1:p.Glu159=
NM_006415.3:c.477A=	NP_006406.1:p.Glu159=
XM_011518138.1:c.477A=	XP_011516440.1:p.Glu159=
XM_011518139.1:c.12A=	XP_011516441.1:p.Glu4=
XM_011518138.2:c.477A=	XP_011516440.1:p.Glu159=
XM_011518139.3:c.12A=	XP_011516441.1:p.Glu4=
XM_017014200.2:c.111A=	XP_016869689.1:p.Glu37=
XM_017014201.2:c.111A=	XP_016869690.1:p.Glu37=
XM_024447378.1:c.12A=	XP_024303146.1:p.Glu4=
XM_024447379.1:c.12A=	XP_024303147.1:p.Glu4=
XR_002956744.1:n.627A=
NM_006415.4:c.477A= MANE Select	NP_006406.1:p.Glu159=
NM_001281303.2:c.477A=	NP_001268232.1:p.Glu159=
NM_001368272.1:c.111A=	NP_001355201.1:p.Glu37=
NM_001368273.1:c.12A=	NP_001355202.1:p.Glu4=