Canonical Allele Identifier: CA7542129

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• dbSNP Id: rs769366321
• ExAC: 15:45554319 AT / A
• gnomAD v2: 15-45554319-AT-A
• gnomAD v3: 15-45262121-AT-A
• gnomAD v4: 15-45262121-AT-A
• MyVariant Identifiers: chr15:g.45554320del (hg19) ; chr15:g.45262122del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45262123del , CM000677.2:g.45262123del	GRCh38
NC_000015.9:g.45554321del , CM000677.1:g.45554321del	GRCh37
NC_000015.8:g.43341613del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347644.8:c.262+17del (SLC28A2) MANE Select	ENSP00000315006.4:n.262+17del
ENST00000347644.7:c.262+17del (SLC28A2)	ENSP00000315006.4:n.262+17del
ENST00000560438.5:c.226+17del (SLC28A2)	ENSP00000454074.1:n.226+17del
NM_004212.3:c.262+17del (SLC28A2)	NP_004203.2:n.262+17del
NR_120335.1:n.27-6124del (SLC28A2-AS1)
XM_011522198.1:c.262+17del (SLC28A2)	XP_011520500.1:n.262+17del
XM_011522199.1:c.262+17del (SLC28A2)	XP_011520501.1:n.262+17del
XM_011522200.1:c.262+17del (SLC28A2)	XP_011520502.1:n.262+17del
XM_011522201.1:c.262+17del (SLC28A2)	XP_011520503.1:n.262+17del
XM_011522198.2:c.262+17del (SLC28A2)	XP_011520500.1:n.262+17del
XM_011522200.2:c.262+17del (SLC28A2)	XP_011520502.1:n.262+17del
XM_011522201.2:c.262+17del (SLC28A2)	XP_011520503.1:n.262+17del
NM_004212.4:c.262+17del (SLC28A2) MANE Select	NP_004203.2:n.262+17del