Canonical Allele Identifier: CA373788837

Gene: SPTLC1

Linked Data

• MyVariant Identifiers: chr9:g.94794749A>T (hg19) ; chr9:g.92032467A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92032467A>T , CM000671.2:g.92032467A>T	GRCh38
NC_000009.11:g.94794749A>T , CM000671.1:g.94794749A>T	GRCh37
NC_000009.10:g.93834570A>T	NCBI36
NG_007950.1:g.87942T>A , LRG_272:g.87942T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686600.1:c.*132T>A	ENSP00000509268.1:n.*132T>A
ENST00000686799.1:n.1744T>A
ENST00000687427.1:c.*176T>A	ENSP00000509426.1:n.*176T>A
ENST00000687817.1:c.*3818T>A	ENSP00000508926.1:n.*3818T>A
ENST00000687972.1:c.1480T>A	ENSP00000509208.1:p.Ter494Lys
ENST00000689261.1:n.1327T>A
ENST00000689401.1:c.*1670T>A	ENSP00000510251.1:n.*1670T>A
ENST00000690095.1:n.1808T>A
ENST00000690139.1:c.*1121T>A	ENSP00000510483.1:n.*1121T>A
ENST00000692458.1:n.2058T>A
ENST00000262554.7:c.1420T>A MANE Select	ENSP00000262554.2:p.Ter474Lys
ENST00000642671.1:c.1629+2343T>A	ENSP00000495764.1:n.1629+2343T>A
ENST00000643599.1:c.1396+2343T>A	ENSP00000494770.1:n.1396+2343T>A
ENST00000644140.1:c.*1161T>A	ENSP00000493933.1:n.*1161T>A
ENST00000646481.1:c.1260+2343T>A	ENSP00000496627.1:n.1260+2343T>A
ENST00000646534.1:c.*1223T>A	ENSP00000495388.1:n.*1223T>A
ENST00000262554.6:c.1420T>A	ENSP00000262554.2:p.Ter474Lys
ENST00000469778.1:n.377T>A
NM_001281303.1:c.1388T>A	NP_001268232.1:p.Leu463Gln
NM_006415.3:c.1420T>A	NP_006406.1:p.Ter474Lys
XM_011518139.1:c.955T>A	XP_011516441.1:p.Ter319Lys
XM_011518139.3:c.955T>A	XP_011516441.1:p.Ter319Lys
XM_017014200.2:c.1054T>A	XP_016869689.1:p.Ter352Lys
XM_017014201.2:c.1054T>A	XP_016869690.1:p.Ter352Lys
XM_024447378.1:c.955T>A	XP_024303146.1:p.Ter319Lys
XM_024447379.1:c.955T>A	XP_024303147.1:p.Ter319Lys
XR_002956744.1:n.1570T>A
NM_006415.4:c.1420T>A MANE Select	NP_006406.1:p.Ter474Lys
NM_001281303.2:c.1388T>A	NP_001268232.1:p.Leu463Gln
NM_001368272.1:c.1054T>A	NP_001355201.1:p.Ter352Lys
NM_001368273.1:c.955T>A	NP_001355202.1:p.Ter319Lys