Canonical Allele Identifier: CA2148430700
Gene: SPTLC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.77518097T= , CM000676.2:g.77518097T= GRCh38
NC_000014.8:g.77984440T= , CM000676.1:g.77984440T= GRCh37
NC_000014.7:g.77054193T= NCBI36
NG_028282.1:g.103671A= , LRG_371:g.103671A=

Transcript Alleles

HGVS Amino-acid change
ENST00000686627.1:n.542A=
ENST00000687688.1:n.1273A=
ENST00000692906.1:n.1242A=
ENST00000216484.7:c.1510A= MANE Select ENSP00000216484.2:p.Ile504=
ENST00000216484.6:c.1510A= ENSP00000216484.2:p.Ile504=
ENST00000556607.1:c.338A= ENSP00000451029.1:n.338A=
NM_004863.3:c.1510A= , LRG_371t1:c.1510A= NP_004854.1:p.Ile504=
NM_004863.4:c.1510A= MANE Select NP_004854.1:p.Ile504=