Canonical Allele Identifier: CA2628262775

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• gnomAD v4: 15-45262160-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45262160C>A , CM000677.2:g.45262160C>A	GRCh38
NC_000015.9:g.45554358C>A , CM000677.1:g.45554358C>A	GRCh37
NC_000015.8:g.43341650C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347644.8:c.262+54C>A (SLC28A2) MANE Select	ENSP00000315006.4:n.262+54C>A
ENST00000347644.7:c.262+54C>A (SLC28A2)	ENSP00000315006.4:n.262+54C>A
ENST00000560438.5:c.226+54C>A (SLC28A2)	ENSP00000454074.1:n.226+54C>A
NM_004212.3:c.262+54C>A (SLC28A2)	NP_004203.2:n.262+54C>A
NR_120335.1:n.27-6162G>T (SLC28A2-AS1)
XM_011522198.1:c.262+54C>A (SLC28A2)	XP_011520500.1:n.262+54C>A
XM_011522199.1:c.262+54C>A (SLC28A2)	XP_011520501.1:n.262+54C>A
XM_011522200.1:c.262+54C>A (SLC28A2)	XP_011520502.1:n.262+54C>A
XM_011522201.1:c.262+54C>A (SLC28A2)	XP_011520503.1:n.262+54C>A
XM_011522198.2:c.262+54C>A (SLC28A2)	XP_011520500.1:n.262+54C>A
XM_011522200.2:c.262+54C>A (SLC28A2)	XP_011520502.1:n.262+54C>A
XM_011522201.2:c.262+54C>A (SLC28A2)	XP_011520503.1:n.262+54C>A
NM_004212.4:c.262+54C>A (SLC28A2) MANE Select	NP_004203.2:n.262+54C>A