Canonical Allele Identifier: CA2579378275

Gene: SPTLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92038213_92038215del , CM000671.2:g.92038213_92038215del	GRCh38
NC_000009.11:g.94800495_94800497del , CM000671.1:g.94800495_94800497del	GRCh37
NC_000009.10:g.93840316_93840318del	NCBI36
NG_007950.1:g.82197_82199del , LRG_272:g.82197_82199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482632.6:n.1664+36_1664+38del
ENST00000686600.1:c.1254+36_1254+38del	ENSP00000509268.1:n.1254+36_1254+38del
ENST00000686799.1:n.1351+36_1351+38del
ENST00000687427.1:c.1254+36_1254+38del	ENSP00000509426.1:n.1254+36_1254+38del
ENST00000687817.1:c.*1401+36_*1401+38del	ENSP00000508926.1:n.*1401+36_*1401+38del
ENST00000687972.1:c.1314+36_1314+38del	ENSP00000509208.1:n.1314+36_1314+38del
ENST00000689261.1:n.1161+36_1161+38del
ENST00000689401.1:c.*1504+36_*1504+38del	ENSP00000510251.1:n.*1504+36_*1504+38del
ENST00000689423.1:c.*1504+36_*1504+38del	ENSP00000508519.1:n.*1504+36_*1504+38del
ENST00000690095.1:n.1642+36_1642+38del
ENST00000690139.1:c.*955+36_*955+38del	ENSP00000510483.1:n.*955+36_*955+38del
ENST00000692458.1:n.1621+36_1621+38del
ENST00000693147.1:c.*1270+36_*1270+38del	ENSP00000510358.1:n.*1270+36_*1270+38del
ENST00000262554.7:c.1254+36_1254+38del MANE Select	ENSP00000262554.2:n.1254+36_1254+38del
ENST00000642671.1:c.1555+36_1555+38del	ENSP00000495764.1:n.1555+36_1555+38del
ENST00000643599.1:c.1322+36_1322+38del	ENSP00000494770.1:n.1322+36_1322+38del
ENST00000644140.1:c.*995+36_*995+38del	ENSP00000493933.1:n.*995+36_*995+38del
ENST00000646481.1:c.1186+36_1186+38del	ENSP00000496627.1:n.1186+36_1186+38del
ENST00000646534.1:c.*1057+36_*1057+38del	ENSP00000495388.1:n.*1057+36_*1057+38del
ENST00000262554.6:c.1254+36_1254+38del	ENSP00000262554.2:n.1254+36_1254+38del
ENST00000469778.1:n.211+36_211+38del
NM_001281303.1:c.1254+36_1254+38del	NP_001268232.1:n.1254+36_1254+38del
NM_006415.3:c.1254+36_1254+38del	NP_006406.1:n.1254+36_1254+38del
XM_011518139.1:c.789+36_789+38del	XP_011516441.1:n.789+36_789+38del
XM_011518139.3:c.789+36_789+38del	XP_011516441.1:n.789+36_789+38del
XM_017014200.2:c.888+36_888+38del	XP_016869689.1:n.888+36_888+38del
XM_017014201.2:c.888+36_888+38del	XP_016869690.1:n.888+36_888+38del
XM_024447378.1:c.789+36_789+38del	XP_024303146.1:n.789+36_789+38del
XM_024447379.1:c.789+36_789+38del	XP_024303147.1:n.789+36_789+38del
XR_002956744.1:n.1404+36_1404+38del
NM_006415.4:c.1254+36_1254+38del MANE Select	NP_006406.1:n.1254+36_1254+38del
NM_001281303.2:c.1254+36_1254+38del	NP_001268232.1:n.1254+36_1254+38del
NM_001368272.1:c.888+36_888+38del	NP_001355201.1:n.888+36_888+38del
NM_001368273.1:c.789+36_789+38del	NP_001355202.1:n.789+36_789+38del