Canonical Allele Identifier: CA390699885

Gene: SPTLC2

Linked Data

• MyVariant Identifiers: chr14:g.77984427G>T (hg19) ; chr14:g.77518084G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77518084G>T , CM000676.2:g.77518084G>T	GRCh38
NC_000014.8:g.77984427G>T , CM000676.1:g.77984427G>T	GRCh37
NC_000014.7:g.77054180G>T	NCBI36
NG_028282.1:g.103684C>A , LRG_371:g.103684C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686627.1:n.555C>A
ENST00000687688.1:n.1286C>A
ENST00000692906.1:n.1255C>A
ENST00000216484.7:c.1523C>A MANE Select	ENSP00000216484.2:p.Ala508Asp
ENST00000216484.6:c.1523C>A	ENSP00000216484.2:p.Ala508Asp
ENST00000556607.1:c.351C>A	ENSP00000451029.1:n.351C>A
NM_004863.3:c.1523C>A , LRG_371t1:c.1523C>A	NP_004854.1:p.Ala508Asp
NM_004863.4:c.1523C>A MANE Select	NP_004854.1:p.Ala508Asp