Canonical Allele Identifier: CA490225006

Gene: SLC28A2 SLC28A2-AS1

Linked Data

• MyVariant Identifiers: chr15:g.45545482G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45253284G>C , CM000677.2:g.45253284G>C	GRCh38
NC_000015.9:g.45545482G>C , CM000677.1:g.45545482G>C	GRCh37
NC_000015.8:g.43332774G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000347644.8:c.69G>C (SLC28A2) MANE Select	ENSP00000315006.4:p.Gly23=
ENST00000347644.7:c.69G>C (SLC28A2)	ENSP00000315006.4:p.Gly23=
ENST00000560438.5:c.46-148G>C (SLC28A2)	ENSP00000454074.1:n.46-148G>C
NM_004212.3:c.69G>C (SLC28A2)	NP_004203.2:p.Gly23=
NR_120335.1:n.180+582C>G (SLC28A2-AS1)
XM_011522198.1:c.69G>C (SLC28A2)	XP_011520500.1:p.Gly23=
XM_011522199.1:c.69G>C (SLC28A2)	XP_011520501.1:p.Gly23=
XM_011522200.1:c.69G>C (SLC28A2)	XP_011520502.1:p.Gly23=
XM_011522201.1:c.69G>C (SLC28A2)	XP_011520503.1:p.Gly23=
XM_011522198.2:c.69G>C (SLC28A2)	XP_011520500.1:p.Gly23=
XM_011522200.2:c.69G>C (SLC28A2)	XP_011520502.1:p.Gly23=
XM_011522201.2:c.69G>C (SLC28A2)	XP_011520503.1:p.Gly23=
NM_004212.4:c.69G>C (SLC28A2) MANE Select	NP_004203.2:p.Gly23=