Canonical Allele Identifier: CA490218176

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• MyVariant Identifiers: chr15:g.45554288G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45262090G>A , CM000677.2:g.45262090G>A	GRCh38
NC_000015.9:g.45554288G>A , CM000677.1:g.45554288G>A	GRCh37
NC_000015.8:g.43341580G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347644.8:c.246G>A (SLC28A2) MANE Select	ENSP00000315006.4:p.Leu82=
ENST00000347644.7:c.246G>A (SLC28A2)	ENSP00000315006.4:p.Leu82=
ENST00000560438.5:c.210G>A (SLC28A2)	ENSP00000454074.1:p.Leu70=
NM_004212.3:c.246G>A (SLC28A2)	NP_004203.2:p.Leu82=
NR_120335.1:n.27-6092C>T (SLC28A2-AS1)
XM_011522198.1:c.246G>A (SLC28A2)	XP_011520500.1:p.Leu82=
XM_011522199.1:c.246G>A (SLC28A2)	XP_011520501.1:p.Leu82=
XM_011522200.1:c.246G>A (SLC28A2)	XP_011520502.1:p.Leu82=
XM_011522201.1:c.246G>A (SLC28A2)	XP_011520503.1:p.Leu82=
XM_011522198.2:c.246G>A (SLC28A2)	XP_011520500.1:p.Leu82=
XM_011522200.2:c.246G>A (SLC28A2)	XP_011520502.1:p.Leu82=
XM_011522201.2:c.246G>A (SLC28A2)	XP_011520503.1:p.Leu82=
NM_004212.4:c.246G>A (SLC28A2) MANE Select	NP_004203.2:p.Leu82=