Canonical Allele Identifier: CA392251738

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• MyVariant Identifiers: chr15:g.45559675G>C (hg19) ; chr15:g.45267477G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45267477G>C , CM000677.2:g.45267477G>C	GRCh38
NC_000015.9:g.45559675G>C , CM000677.1:g.45559675G>C	GRCh37
NC_000015.8:g.43346967G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000347644.8:c.965G>C (SLC28A2) MANE Select	ENSP00000315006.4:p.Arg322Pro
ENST00000347644.7:c.965G>C (SLC28A2)	ENSP00000315006.4:p.Arg322Pro
ENST00000559924.1:c.579G>C (SLC28A2)
NM_004212.3:c.965G>C (SLC28A2)	NP_004203.2:p.Arg322Pro
NR_120335.1:n.27-11479C>G (SLC28A2-AS1)
XM_011522198.1:c.965G>C (SLC28A2)	XP_011520500.1:p.Arg322Pro
XM_011522199.1:c.965G>C (SLC28A2)	XP_011520501.1:p.Arg322Pro
XM_011522200.1:c.965G>C (SLC28A2)	XP_011520502.1:p.Arg322Pro
XM_011522201.1:c.965G>C (SLC28A2)	XP_011520503.1:p.Arg322Pro
XM_011522202.1:c.80G>C (SLC28A2)	XP_011520504.1:p.Arg27Pro
XM_011522198.2:c.965G>C (SLC28A2)	XP_011520500.1:p.Arg322Pro
XM_011522200.2:c.965G>C (SLC28A2)	XP_011520502.1:p.Arg322Pro
XM_011522201.2:c.965G>C (SLC28A2)	XP_011520503.1:p.Arg322Pro
XM_011522202.2:c.80G>C (SLC28A2)	XP_011520504.1:p.Arg27Pro
NM_004212.4:c.965G>C (SLC28A2) MANE Select	NP_004203.2:p.Arg322Pro