Canonical Allele Identifier: CA2174015708

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• dbSNP Id: rs1900180587
• gnomAD v4: 15-45262112-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45262112A>T , CM000677.2:g.45262112A>T	GRCh38
NC_000015.9:g.45554310A>T , CM000677.1:g.45554310A>T	GRCh37
NC_000015.8:g.43341602A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347644.8:c.262+6A>T (SLC28A2) MANE Select	ENSP00000315006.4:n.262+6A>T
ENST00000347644.7:c.262+6A>T (SLC28A2)	ENSP00000315006.4:n.262+6A>T
ENST00000560438.5:c.226+6A>T (SLC28A2)	ENSP00000454074.1:n.226+6A>T
NM_004212.3:c.262+6A>T (SLC28A2)	NP_004203.2:n.262+6A>T
NR_120335.1:n.27-6114T>A (SLC28A2-AS1)
XM_011522198.1:c.262+6A>T (SLC28A2)	XP_011520500.1:n.262+6A>T
XM_011522199.1:c.262+6A>T (SLC28A2)	XP_011520501.1:n.262+6A>T
XM_011522200.1:c.262+6A>T (SLC28A2)	XP_011520502.1:n.262+6A>T
XM_011522201.1:c.262+6A>T (SLC28A2)	XP_011520503.1:n.262+6A>T
XM_011522198.2:c.262+6A>T (SLC28A2)	XP_011520500.1:n.262+6A>T
XM_011522200.2:c.262+6A>T (SLC28A2)	XP_011520502.1:n.262+6A>T
XM_011522201.2:c.262+6A>T (SLC28A2)	XP_011520503.1:n.262+6A>T
NM_004212.4:c.262+6A>T (SLC28A2) MANE Select	NP_004203.2:n.262+6A>T