Canonical Allele Identifier: CA2148430681
Gene: SPTLC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77518039G= , CM000676.2:g.77518039G= GRCh38
NC_000014.8:g.77984382G= , CM000676.1:g.77984382G= GRCh37
NC_000014.7:g.77054135G= NCBI36
NG_028282.1:g.103729C= , LRG_371:g.103729C=

Transcript Alleles

HGVS Amino-acid change
ENST00000686627.1:n.600C=
ENST00000687688.1:n.1331C=
ENST00000692906.1:n.1300C=
ENST00000216484.7:c.1568C= MANE Select ENSP00000216484.2:p.Thr523=
ENST00000216484.6:c.1568C= ENSP00000216484.2:p.Thr523=
ENST00000556607.1:c.396C= ENSP00000451029.1:n.396C=
NM_004863.3:c.1568C= , LRG_371t1:c.1568C= NP_004854.1:p.Thr523=
NM_004863.4:c.1568C= MANE Select NP_004854.1:p.Thr523=