Canonical Allele Identifier: CA2690639733

Gene: SPTLC1

Linked Data

• gnomAD v4: 9-92067820-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92067820_92067821insG , CM000671.2:g.92067820_92067821insG	GRCh38
NC_000009.11:g.94830102_94830103insG , CM000671.1:g.94830102_94830103insG	GRCh37
NC_000009.10:g.93869923_93869924insG	NCBI36
NG_007950.1:g.52588_52589insC , LRG_272:g.52588_52589insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482632.6:n.970+145_970+146insC
ENST00000686600.1:c.560+145_560+146insC	ENSP00000509268.1:n.560+145_560+146insC
ENST00000686799.1:n.657+145_657+146insC
ENST00000687427.1:c.560+145_560+146insC	ENSP00000509426.1:n.560+145_560+146insC
ENST00000687817.1:c.*363+145_*363+146insC	ENSP00000508926.1:n.*363+145_*363+146insC
ENST00000687972.1:c.620+145_620+146insC	ENSP00000509208.1:n.620+145_620+146insC
ENST00000689261.1:n.467+145_467+146insC
ENST00000689401.1:c.*810+145_*810+146insC	ENSP00000510251.1:n.*810+145_*810+146insC
ENST00000689423.1:c.*810+145_*810+146insC	ENSP00000508519.1:n.*810+145_*810+146insC
ENST00000690095.1:n.888+145_888+146insC
ENST00000690139.1:c.*261+145_*261+146insC	ENSP00000510483.1:n.*261+145_*261+146insC
ENST00000692458.1:n.583+145_583+146insC
ENST00000693147.1:c.*576+145_*576+146insC	ENSP00000510358.1:n.*576+145_*576+146insC
ENST00000262554.7:c.560+145_560+146insC MANE Select	ENSP00000262554.2:n.560+145_560+146insC
ENST00000642671.1:c.605+145_605+146insC	ENSP00000495764.1:n.605+145_605+146insC
ENST00000643599.1:c.432+145_432+146insC	ENSP00000494770.1:n.432+145_432+146insC
ENST00000644140.1:c.*301+145_*301+146insC	ENSP00000493933.1:n.*301+145_*301+146insC
ENST00000646481.1:c.432+145_432+146insC	ENSP00000496627.1:n.432+145_432+146insC
ENST00000646534.1:c.*363+145_*363+146insC	ENSP00000495388.1:n.*363+145_*363+146insC
ENST00000262554.6:c.560+145_560+146insC	ENSP00000262554.2:n.560+145_560+146insC
ENST00000482632.5:n.707+145_707+146insC
NM_001281303.1:c.560+145_560+146insC	NP_001268232.1:n.560+145_560+146insC
NM_006415.3:c.560+145_560+146insC	NP_006406.1:n.560+145_560+146insC
XM_011518138.1:c.560+145_560+146insC	XP_011516440.1:n.560+145_560+146insC
XM_011518139.1:c.95+145_95+146insC	XP_011516441.1:n.95+145_95+146insC
XM_011518138.2:c.560+145_560+146insC	XP_011516440.1:n.560+145_560+146insC
XM_011518139.3:c.95+145_95+146insC	XP_011516441.1:n.95+145_95+146insC
XM_017014200.2:c.194+145_194+146insC	XP_016869689.1:n.194+145_194+146insC
XM_017014201.2:c.194+145_194+146insC	XP_016869690.1:n.194+145_194+146insC
XM_024447378.1:c.95+145_95+146insC	XP_024303146.1:n.95+145_95+146insC
XM_024447379.1:c.95+145_95+146insC	XP_024303147.1:n.95+145_95+146insC
XR_002956744.1:n.710+145_710+146insC
NM_006415.4:c.560+145_560+146insC MANE Select	NP_006406.1:n.560+145_560+146insC
NM_001281303.2:c.560+145_560+146insC	NP_001268232.1:n.560+145_560+146insC
NM_001368272.1:c.194+145_194+146insC	NP_001355201.1:n.194+145_194+146insC
NM_001368273.1:c.95+145_95+146insC	NP_001355202.1:n.95+145_95+146insC