Canonical Allele Identifier: CA390699851

Gene: SPTLC2

Linked Data

• MyVariant Identifiers: chr14:g.77984420A>T (hg19) ; chr14:g.77518077A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77518077A>T , CM000676.2:g.77518077A>T	GRCh38
NC_000014.8:g.77984420A>T , CM000676.1:g.77984420A>T	GRCh37
NC_000014.7:g.77054173A>T	NCBI36
NG_028282.1:g.103691T>A , LRG_371:g.103691T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686627.1:n.562T>A
ENST00000687688.1:n.1293T>A
ENST00000692906.1:n.1262T>A
ENST00000216484.7:c.1530T>A MANE Select	ENSP00000216484.2:p.Phe510Leu
ENST00000216484.6:c.1530T>A	ENSP00000216484.2:p.Phe510Leu
ENST00000556607.1:c.358T>A	ENSP00000451029.1:n.358T>A
NM_004863.3:c.1530T>A , LRG_371t1:c.1530T>A	NP_004854.1:p.Phe510Leu
NM_004863.4:c.1530T>A MANE Select	NP_004854.1:p.Phe510Leu