Canonical Allele Identifier: CA2176303569

Gene: SLC27A2

Linked Data

• dbSNP Id: rs12913823

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50217394C>A , CM000677.2:g.50217394C>A	GRCh38
NC_000015.9:g.50509591C>A , CM000677.1:g.50509591C>A	GRCh37
NC_000015.8:g.48296883C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000267842.10:c.973-5571C>A MANE Select	ENSP00000267842.5:n.973-5571C>A
ENST00000267842.9:c.973-5571C>A	ENSP00000267842.5:n.973-5571C>A
ENST00000380902.8:c.814-5571C>A	ENSP00000370289.4:n.814-5571C>A
ENST00000544960.1:c.268-5571C>A	ENSP00000444549.1:n.268-5571C>A
ENST00000559938.1:n.12-5571C>A
NM_001159629.1:c.814-5571C>A	NP_001153101.1:n.814-5571C>A
NM_003645.3:c.973-5571C>A	NP_003636.2:n.973-5571C>A
NM_003645.4:c.973-5571C>A MANE Select	NP_003636.2:n.973-5571C>A
NM_001159629.2:c.814-5571C>A	NP_001153101.1:n.814-5571C>A