Canonical Allele Identifier: CA2174011524
Gene: SLC28A2 HGNC NCBI
SLC28A2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45253283G= , CM000677.2:g.45253283G= GRCh38
NC_000015.9:g.45545481G= , CM000677.1:g.45545481G= GRCh37
NC_000015.8:g.43332773G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000347644.8:c.68G= (SLC28A2) MANE Select ENSP00000315006.4:p.Gly23=
ENST00000347644.7:c.68G= (SLC28A2) ENSP00000315006.4:p.Gly23=
ENST00000560438.5:c.46-149G= (SLC28A2) ENSP00000454074.1:n.46-149G=
NM_004212.3:c.68G= (SLC28A2) NP_004203.2:p.Gly23=
NR_120335.1:n.180+583C= (SLC28A2-AS1)
XM_011522198.1:c.68G= (SLC28A2) XP_011520500.1:p.Gly23=
XM_011522199.1:c.68G= (SLC28A2) XP_011520501.1:p.Gly23=
XM_011522200.1:c.68G= (SLC28A2) XP_011520502.1:p.Gly23=
XM_011522201.1:c.68G= (SLC28A2) XP_011520503.1:p.Gly23=
XM_011522198.2:c.68G= (SLC28A2) XP_011520500.1:p.Gly23=
XM_011522200.2:c.68G= (SLC28A2) XP_011520502.1:p.Gly23=
XM_011522201.2:c.68G= (SLC28A2) XP_011520503.1:p.Gly23=
NM_004212.4:c.68G= (SLC28A2) MANE Select NP_004203.2:p.Gly23=