Canonical Allele Identifier: CA2176303568

Gene: SLC27A2

Genomic Alleles

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

Transcript Alleles

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