Canonical Allele Identifier: CA1864080829

Gene: SPTLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92067909_92067913delinsACAGT , CM000671.2:g.92067909_92067913delinsACAGT	GRCh38
NC_000009.11:g.94830191_94830195delinsACAGT , CM000671.1:g.94830191_94830195delinsACAGT	GRCh37
NC_000009.10:g.93870012_93870016delinsACAGT	NCBI36
NG_007950.1:g.52496_52500delinsACTGT , LRG_272:g.52496_52500delinsACTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000482632.6:n.970+53_970+57delinsACTGT
ENST00000686600.1:c.560+53_560+57delinsACTGT	ENSP00000509268.1:n.560+53_560+57delinsACTGT
ENST00000686799.1:n.657+53_657+57delinsACTGT
ENST00000687427.1:c.560+53_560+57delinsACTGT	ENSP00000509426.1:n.560+53_560+57delinsACTGT
ENST00000687817.1:c.*363+53_*363+57delinsACTGT	ENSP00000508926.1:n.*363+53_*363+57delinsACTGT
ENST00000687972.1:c.620+53_620+57delinsACTGT	ENSP00000509208.1:n.620+53_620+57delinsACTGT
ENST00000689261.1:n.467+53_467+57delinsACTGT
ENST00000689401.1:c.*810+53_*810+57delinsACTGT	ENSP00000510251.1:n.*810+53_*810+57delinsACTGT
ENST00000689423.1:c.*810+53_*810+57delinsACTGT	ENSP00000508519.1:n.*810+53_*810+57delinsACTGT
ENST00000690095.1:n.888+53_888+57delinsACTGT
ENST00000690139.1:c.*261+53_*261+57delinsACTGT	ENSP00000510483.1:n.*261+53_*261+57delinsACTGT
ENST00000692458.1:n.583+53_583+57delinsACTGT
ENST00000693147.1:c.*576+53_*576+57delinsACTGT	ENSP00000510358.1:n.*576+53_*576+57delinsACTGT
ENST00000262554.7:c.560+53_560+57delinsACTGT MANE Select	ENSP00000262554.2:n.560+53_560+57delinsACTGT
ENST00000642671.1:c.605+53_605+57delinsACTGT	ENSP00000495764.1:n.605+53_605+57delinsACTGT
ENST00000643599.1:c.432+53_432+57delinsACTGT	ENSP00000494770.1:n.432+53_432+57delinsACTGT
ENST00000644140.1:c.*301+53_*301+57delinsACTGT	ENSP00000493933.1:n.*301+53_*301+57delinsACTGT
ENST00000646481.1:c.432+53_432+57delinsACTGT	ENSP00000496627.1:n.432+53_432+57delinsACTGT
ENST00000646534.1:c.*363+53_*363+57delinsACTGT	ENSP00000495388.1:n.*363+53_*363+57delinsACTGT
ENST00000262554.6:c.560+53_560+57delinsACTGT	ENSP00000262554.2:n.560+53_560+57delinsACTGT
ENST00000482632.5:n.707+53_707+57delinsACTGT
NM_001281303.1:c.560+53_560+57delinsACTGT	NP_001268232.1:n.560+53_560+57delinsACTGT
NM_006415.3:c.560+53_560+57delinsACTGT	NP_006406.1:n.560+53_560+57delinsACTGT
XM_011518138.1:c.560+53_560+57delinsACTGT	XP_011516440.1:n.560+53_560+57delinsACTGT
XM_011518139.1:c.95+53_95+57delinsACTGT	XP_011516441.1:n.95+53_95+57delinsACTGT
XM_011518138.2:c.560+53_560+57delinsACTGT	XP_011516440.1:n.560+53_560+57delinsACTGT
XM_011518139.3:c.95+53_95+57delinsACTGT	XP_011516441.1:n.95+53_95+57delinsACTGT
XM_017014200.2:c.194+53_194+57delinsACTGT	XP_016869689.1:n.194+53_194+57delinsACTGT
XM_017014201.2:c.194+53_194+57delinsACTGT	XP_016869690.1:n.194+53_194+57delinsACTGT
XM_024447378.1:c.95+53_95+57delinsACTGT	XP_024303146.1:n.95+53_95+57delinsACTGT
XM_024447379.1:c.95+53_95+57delinsACTGT	XP_024303147.1:n.95+53_95+57delinsACTGT
XR_002956744.1:n.710+53_710+57delinsACTGT
NM_006415.4:c.560+53_560+57delinsACTGT MANE Select	NP_006406.1:n.560+53_560+57delinsACTGT
NM_001281303.2:c.560+53_560+57delinsACTGT	NP_001268232.1:n.560+53_560+57delinsACTGT
NM_001368272.1:c.194+53_194+57delinsACTGT	NP_001355201.1:n.194+53_194+57delinsACTGT
NM_001368273.1:c.95+53_95+57delinsACTGT	NP_001355202.1:n.95+53_95+57delinsACTGT