Canonical Allele Identifier: CA2174018051

Gene: SLC28A2 SLC28A2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45267576T= , CM000677.2:g.45267576T=	GRCh38
NC_000015.9:g.45559774T= , CM000677.1:g.45559774T=	GRCh37
NC_000015.8:g.43347066T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004212.4:c.1064T= (SLC28A2) MANE Select	NP_004203.2:p.Phe355=
ENST00000347644.8:c.1064T= (SLC28A2) MANE Select	ENSP00000315006.4:p.Phe355=
NM_004212.3:c.1064T= (SLC28A2)	NP_004203.2:p.Phe355=
NR_120335.1:n.27-11578A= (SLC28A2-AS1)
ENST00000347644.7:c.1064T= (SLC28A2)	ENSP00000315006.4:p.Phe355=
ENST00000559924.1:c.678T= (SLC28A2)
XM_011522198.1:c.1064T= (SLC28A2)	XP_011520500.1:p.Phe355=
XM_011522198.2:c.1064T= (SLC28A2)	XP_011520500.1:p.Phe355=
XM_011522199.1:c.1064T= (SLC28A2)	XP_011520501.1:p.Phe355=
XM_011522200.1:c.1064T= (SLC28A2)	XP_011520502.1:p.Phe355=
XM_011522200.2:c.1064T= (SLC28A2)	XP_011520502.1:p.Phe355=
XM_011522201.1:c.1064T= (SLC28A2)	XP_011520503.1:p.Phe355=
XM_011522201.2:c.1064T= (SLC28A2)	XP_011520503.1:p.Phe355=
XM_011522202.1:c.179T= (SLC28A2)	XP_011520504.1:p.Phe60=
XM_011522202.2:c.179T= (SLC28A2)	XP_011520504.1:p.Phe60=