Canonical Allele Identifier: CA2690637389

Gene: SPTLC1

Linked Data

• gnomAD v4: 9-92032404-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92032407del , CM000671.2:g.92032407del	GRCh38
NC_000009.11:g.94794689del , CM000671.1:g.94794689del	GRCh37
NC_000009.10:g.93834510del	NCBI36
NG_007950.1:g.88004del , LRG_272:g.88004del

Transcript Alleles

HGVS	Amino-acid change
ENST00000686600.1:c.*194del	ENSP00000509268.1:n.*194del
ENST00000686799.1:n.1806del
ENST00000687427.1:c.*238del	ENSP00000509426.1:n.*238del
ENST00000687817.1:c.*3880del	ENSP00000508926.1:n.*3880del
ENST00000687972.1:c.*60del	ENSP00000509208.1:n.*60del
ENST00000689261.1:n.1389del
ENST00000689401.1:c.*1732del	ENSP00000510251.1:n.*1732del
ENST00000690095.1:n.1870del
ENST00000690139.1:c.*1183del	ENSP00000510483.1:n.*1183del
ENST00000692458.1:n.2120del
ENST00000262554.7:c.*60del MANE Select	ENSP00000262554.2:n.*60del
ENST00000642671.1:c.1629+2405del	ENSP00000495764.1:n.1629+2405del
ENST00000643599.1:c.1396+2405del	ENSP00000494770.1:n.1396+2405del
ENST00000644140.1:c.*1223del	ENSP00000493933.1:n.*1223del
ENST00000646481.1:c.1260+2405del	ENSP00000496627.1:n.1260+2405del
ENST00000646534.1:c.*1285del	ENSP00000495388.1:n.*1285del
ENST00000262554.6:c.*60del	ENSP00000262554.2:n.*60del
ENST00000469778.1:n.439del
NM_001281303.1:c.1450del	NP_001268232.1:p.Arg484AlafsTer7
NM_006415.3:c.*60del	NP_006406.1:n.*60del
XM_011518139.1:c.*60del	XP_011516441.1:n.*60del
XM_011518139.3:c.*60del	XP_011516441.1:n.*60del
XM_017014200.2:c.*60del	XP_016869689.1:n.*60del
XM_017014201.2:c.*60del	XP_016869690.1:n.*60del
XM_024447378.1:c.*60del	XP_024303146.1:n.*60del
XM_024447379.1:c.*60del	XP_024303147.1:n.*60del
XR_002956744.1:n.1632del
NM_006415.4:c.*60del MANE Select	NP_006406.1:n.*60del
NM_001281303.2:c.1450del	NP_001268232.1:p.Arg484AlafsTer7
NM_001368272.1:c.*60del	NP_001355201.1:n.*60del
NM_001368273.1:c.*60del	NP_001355202.1:n.*60del