Canonical Allele Identifier: CA487325256

Gene: SPTLC2

Linked Data

• MyVariant Identifiers: chr14:g.77984423C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77518080C>T , CM000676.2:g.77518080C>T	GRCh38
NC_000014.8:g.77984423C>T , CM000676.1:g.77984423C>T	GRCh37
NC_000014.7:g.77054176C>T	NCBI36
NG_028282.1:g.103688G>A , LRG_371:g.103688G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686627.1:n.559G>A
ENST00000687688.1:n.1290G>A
ENST00000692906.1:n.1259G>A
ENST00000216484.7:c.1527G>A MANE Select	ENSP00000216484.2:p.Arg509=
ENST00000216484.6:c.1527G>A	ENSP00000216484.2:p.Arg509=
ENST00000556607.1:c.355G>A	ENSP00000451029.1:n.355G>A
NM_004863.3:c.1527G>A , LRG_371t1:c.1527G>A	NP_004854.1:p.Arg509=
NM_004863.4:c.1527G>A MANE Select	NP_004854.1:p.Arg509=