Canonical Allele Identifier: CA392252372

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• dbSNP Id: rs1243040407
• gnomAD v2: 15-45559777-G-A
• gnomAD v4: 15-45267579-G-A
• MyVariant Identifiers: chr15:g.45559777G>A (hg19) ; chr15:g.45267579G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45267579G>A , CM000677.2:g.45267579G>A	GRCh38
NC_000015.9:g.45559777G>A , CM000677.1:g.45559777G>A	GRCh37
NC_000015.8:g.43347069G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000347644.8:c.1067G>A (SLC28A2) MANE Select	ENSP00000315006.4:p.Gly356Glu
ENST00000347644.7:c.1067G>A (SLC28A2)	ENSP00000315006.4:p.Gly356Glu
ENST00000559924.1:c.681G>A (SLC28A2)
NM_004212.3:c.1067G>A (SLC28A2)	NP_004203.2:p.Gly356Glu
NR_120335.1:n.27-11581C>T (SLC28A2-AS1)
XM_011522198.1:c.1067G>A (SLC28A2)	XP_011520500.1:p.Gly356Glu
XM_011522199.1:c.1067G>A (SLC28A2)	XP_011520501.1:p.Gly356Glu
XM_011522200.1:c.1067G>A (SLC28A2)	XP_011520502.1:p.Gly356Glu
XM_011522201.1:c.1067G>A (SLC28A2)	XP_011520503.1:p.Gly356Glu
XM_011522202.1:c.182G>A (SLC28A2)	XP_011520504.1:p.Gly61Glu
XM_011522198.2:c.1067G>A (SLC28A2)	XP_011520500.1:p.Gly356Glu
XM_011522200.2:c.1067G>A (SLC28A2)	XP_011520502.1:p.Gly356Glu
XM_011522201.2:c.1067G>A (SLC28A2)	XP_011520503.1:p.Gly356Glu
XM_011522202.2:c.182G>A (SLC28A2)	XP_011520504.1:p.Gly61Glu
NM_004212.4:c.1067G>A (SLC28A2) MANE Select	NP_004203.2:p.Gly356Glu