Canonical Allele Identifier: CA1864080908

Gene: SPTLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92067971A= , CM000671.2:g.92067971A=	GRCh38
NC_000009.11:g.94830253A= , CM000671.1:g.94830253A=	GRCh37
NC_000009.10:g.93870074A=	NCBI36
NG_007950.1:g.52438T= , LRG_272:g.52438T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000482632.6:n.965T=
ENST00000686600.1:c.555T=	ENSP00000509268.1:p.Val185=
ENST00000686799.1:n.652T=
ENST00000687427.1:c.555T=	ENSP00000509426.1:p.Val185=
ENST00000687817.1:c.*358T=	ENSP00000508926.1:n.*358T=
ENST00000687972.1:c.615T=	ENSP00000509208.1:p.Val205=
ENST00000689261.1:n.462T=
ENST00000689401.1:c.*805T=	ENSP00000510251.1:n.*805T=
ENST00000689423.1:c.*805T=	ENSP00000508519.1:n.*805T=
ENST00000690095.1:n.883T=
ENST00000690139.1:c.*256T=	ENSP00000510483.1:n.*256T=
ENST00000692458.1:n.578T=
ENST00000693147.1:c.*571T=	ENSP00000510358.1:n.*571T=
ENST00000262554.7:c.555T= MANE Select	ENSP00000262554.2:p.Val185=
ENST00000642671.1:c.600T=	ENSP00000495764.1:n.600T=
ENST00000643599.1:c.427T=	ENSP00000494770.1:n.427T=
ENST00000644140.1:c.*296T=	ENSP00000493933.1:n.*296T=
ENST00000646481.1:c.427T=	ENSP00000496627.1:n.427T=
ENST00000646534.1:c.*358T=	ENSP00000495388.1:n.*358T=
ENST00000262554.6:c.555T=	ENSP00000262554.2:p.Val185=
ENST00000482632.5:n.702T=
NM_001281303.1:c.555T=	NP_001268232.1:p.Val185=
NM_006415.3:c.555T=	NP_006406.1:p.Val185=
XM_011518138.1:c.555T=	XP_011516440.1:p.Val185=
XM_011518139.1:c.90T=	XP_011516441.1:p.Val30=
XM_011518138.2:c.555T=	XP_011516440.1:p.Val185=
XM_011518139.3:c.90T=	XP_011516441.1:p.Val30=
XM_017014200.2:c.189T=	XP_016869689.1:p.Val63=
XM_017014201.2:c.189T=	XP_016869690.1:p.Val63=
XM_024447378.1:c.90T=	XP_024303146.1:p.Val30=
XM_024447379.1:c.90T=	XP_024303147.1:p.Val30=
XR_002956744.1:n.705T=
NM_006415.4:c.555T= MANE Select	NP_006406.1:p.Val185=
NM_001281303.2:c.555T=	NP_001268232.1:p.Val185=
NM_001368272.1:c.189T=	NP_001355201.1:p.Val63=
NM_001368273.1:c.90T=	NP_001355202.1:p.Val30=