Canonical Allele Identifier: CA1864052867
Gene: SPTLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92032397T= , CM000671.2:g.92032397T= GRCh38
NC_000009.11:g.94794679T= , CM000671.1:g.94794679T= GRCh37
NC_000009.10:g.93834500T= NCBI36
NG_007950.1:g.88012A= , LRG_272:g.88012A=

Transcript Alleles

HGVS Amino-acid change
ENST00000686600.1:c.*202A= ENSP00000509268.1:n.*202A=
ENST00000686799.1:n.1814A=
ENST00000687427.1:c.*246A= ENSP00000509426.1:n.*246A=
ENST00000687817.1:c.*3888A= ENSP00000508926.1:n.*3888A=
ENST00000687972.1:c.*68A= ENSP00000509208.1:n.*68A=
ENST00000689261.1:n.1397A=
ENST00000689401.1:c.*1740A= ENSP00000510251.1:n.*1740A=
ENST00000690095.1:n.1878A=
ENST00000690139.1:c.*1191A= ENSP00000510483.1:n.*1191A=
ENST00000692458.1:n.2128A=
ENST00000262554.7:c.*68A= MANE Select ENSP00000262554.2:n.*68A=
ENST00000642671.1:c.1629+2413A= ENSP00000495764.1:n.1629+2413A=
ENST00000643599.1:c.1396+2413A= ENSP00000494770.1:n.1396+2413A=
ENST00000644140.1:c.*1231A= ENSP00000493933.1:n.*1231A=
ENST00000646481.1:c.1260+2413A= ENSP00000496627.1:n.1260+2413A=
ENST00000646534.1:c.*1293A= ENSP00000495388.1:n.*1293A=
ENST00000262554.6:c.*68A= ENSP00000262554.2:n.*68A=
ENST00000469778.1:n.447A=
NM_001281303.1:c.1458A= NP_001268232.1:p.Pro486=
NM_006415.3:c.*68A= NP_006406.1:n.*68A=
XM_011518139.1:c.*68A= XP_011516441.1:n.*68A=
XM_011518139.3:c.*68A= XP_011516441.1:n.*68A=
XM_017014200.2:c.*68A= XP_016869689.1:n.*68A=
XM_017014201.2:c.*68A= XP_016869690.1:n.*68A=
XM_024447378.1:c.*68A= XP_024303146.1:n.*68A=
XM_024447379.1:c.*68A= XP_024303147.1:n.*68A=
XR_002956744.1:n.1640A=
NM_006415.4:c.*68A= MANE Select NP_006406.1:n.*68A=
NM_001281303.2:c.1458A= NP_001268232.1:p.Pro486=
NM_001368272.1:c.*68A= NP_001355201.1:n.*68A=
NM_001368273.1:c.*68A= NP_001355202.1:n.*68A=