Canonical Allele Identifier: CA2803994382

Gene: SLC28A2 SLC28A2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45262103_45262104insGGG , CM000677.2:g.45262103_45262104insGGG	GRCh38
NC_000015.9:g.45554301_45554302insGGG , CM000677.1:g.45554301_45554302insGGG	GRCh37
NC_000015.8:g.43341593_43341594insGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347644.8:c.259_260insGGG (SLC28A2) MANE Select	ENSP00000315006.4:p.Leu87delinsTrpVal
ENST00000347644.7:c.259_260insGGG (SLC28A2)	ENSP00000315006.4:p.Leu87delinsTrpVal
ENST00000560438.5:c.223_224insGGG (SLC28A2)	ENSP00000454074.1:p.Leu75delinsTrpVal
NM_004212.3:c.259_260insGGG (SLC28A2)	NP_004203.2:p.Leu87delinsTrpVal
NR_120335.1:n.27-6106_27-6105insCCC (SLC28A2-AS1)
XM_011522198.1:c.259_260insGGG (SLC28A2)	XP_011520500.1:p.Leu87delinsTrpVal
XM_011522199.1:c.259_260insGGG (SLC28A2)	XP_011520501.1:p.Leu87delinsTrpVal
XM_011522200.1:c.259_260insGGG (SLC28A2)	XP_011520502.1:p.Leu87delinsTrpVal
XM_011522201.1:c.259_260insGGG (SLC28A2)	XP_011520503.1:p.Leu87delinsTrpVal
XM_011522198.2:c.259_260insGGG (SLC28A2)	XP_011520500.1:p.Leu87delinsTrpVal
XM_011522200.2:c.259_260insGGG (SLC28A2)	XP_011520502.1:p.Leu87delinsTrpVal
XM_011522201.2:c.259_260insGGG (SLC28A2)	XP_011520503.1:p.Leu87delinsTrpVal
NM_004212.4:c.259_260insGGG (SLC28A2) MANE Select	NP_004203.2:p.Leu87delinsTrpVal