Canonical Allele Identifier: CA392251779

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• MyVariant Identifiers: chr15:g.45559686G>T (hg19) ; chr15:g.45267488G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45267488G>T , CM000677.2:g.45267488G>T	GRCh38
NC_000015.9:g.45559686G>T , CM000677.1:g.45559686G>T	GRCh37
NC_000015.8:g.43346978G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000347644.8:c.976G>T (SLC28A2) MANE Select	ENSP00000315006.4:p.Gly326Trp
ENST00000347644.7:c.976G>T (SLC28A2)	ENSP00000315006.4:p.Gly326Trp
ENST00000559924.1:c.590G>T (SLC28A2)
NM_004212.3:c.976G>T (SLC28A2)	NP_004203.2:p.Gly326Trp
NR_120335.1:n.27-11490C>A (SLC28A2-AS1)
XM_011522198.1:c.976G>T (SLC28A2)	XP_011520500.1:p.Gly326Trp
XM_011522199.1:c.976G>T (SLC28A2)	XP_011520501.1:p.Gly326Trp
XM_011522200.1:c.976G>T (SLC28A2)	XP_011520502.1:p.Gly326Trp
XM_011522201.1:c.976G>T (SLC28A2)	XP_011520503.1:p.Gly326Trp
XM_011522202.1:c.91G>T (SLC28A2)	XP_011520504.1:p.Gly31Trp
XM_011522198.2:c.976G>T (SLC28A2)	XP_011520500.1:p.Gly326Trp
XM_011522200.2:c.976G>T (SLC28A2)	XP_011520502.1:p.Gly326Trp
XM_011522201.2:c.976G>T (SLC28A2)	XP_011520503.1:p.Gly326Trp
XM_011522202.2:c.91G>T (SLC28A2)	XP_011520504.1:p.Gly31Trp
NM_004212.4:c.976G>T (SLC28A2) MANE Select	NP_004203.2:p.Gly326Trp