Canonical Allele Identifier: CA392246683
Gene: SLC28A2 HGNC NCBI
SLC28A2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45262106G>T , CM000677.2:g.45262106G>T GRCh38
NC_000015.9:g.45554304G>T , CM000677.1:g.45554304G>T GRCh37
NC_000015.8:g.43341596G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347644.8:c.262G>T (SLC28A2) MANE Select ENSP00000315006.4:p.Ala88Ser
ENST00000347644.7:c.262G>T (SLC28A2) ENSP00000315006.4:p.Ala88Ser
ENST00000560438.5:c.226G>T (SLC28A2) ENSP00000454074.1:p.Ala76Ser
NM_004212.3:c.262G>T (SLC28A2) NP_004203.2:p.Ala88Ser
NR_120335.1:n.27-6108C>A (SLC28A2-AS1)
XM_011522198.1:c.262G>T (SLC28A2) XP_011520500.1:p.Ala88Ser
XM_011522199.1:c.262G>T (SLC28A2) XP_011520501.1:p.Ala88Ser
XM_011522200.1:c.262G>T (SLC28A2) XP_011520502.1:p.Ala88Ser
XM_011522201.1:c.262G>T (SLC28A2) XP_011520503.1:p.Ala88Ser
XM_011522198.2:c.262G>T (SLC28A2) XP_011520500.1:p.Ala88Ser
XM_011522200.2:c.262G>T (SLC28A2) XP_011520502.1:p.Ala88Ser
XM_011522201.2:c.262G>T (SLC28A2) XP_011520503.1:p.Ala88Ser
NM_004212.4:c.262G>T (SLC28A2) MANE Select NP_004203.2:p.Ala88Ser