Canonical Allele Identifier: CA2628262025
Gene: SLC28A2 HGNC NCBI
SLC28A2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45253280del , CM000677.2:g.45253280del GRCh38
NC_000015.9:g.45545478del , CM000677.1:g.45545478del GRCh37
NC_000015.8:g.43332770del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000347644.8:c.65del (SLC28A2) MANE Select ENSP00000315006.4:p.Pro22ArgfsTer10
ENST00000347644.7:c.65del (SLC28A2) ENSP00000315006.4:p.Pro22ArgfsTer10
ENST00000560438.5:c.46-152del (SLC28A2) ENSP00000454074.1:n.46-152del
NM_004212.3:c.65del (SLC28A2) NP_004203.2:p.Pro22ArgfsTer10
NR_120335.1:n.180+588del (SLC28A2-AS1)
XM_011522198.1:c.65del (SLC28A2) XP_011520500.1:p.Pro22ArgfsTer10
XM_011522199.1:c.65del (SLC28A2) XP_011520501.1:p.Pro22ArgfsTer10
XM_011522200.1:c.65del (SLC28A2) XP_011520502.1:p.Pro22ArgfsTer10
XM_011522201.1:c.65del (SLC28A2) XP_011520503.1:p.Pro22ArgfsTer10
XM_011522198.2:c.65del (SLC28A2) XP_011520500.1:p.Pro22ArgfsTer10
XM_011522200.2:c.65del (SLC28A2) XP_011520502.1:p.Pro22ArgfsTer10
XM_011522201.2:c.65del (SLC28A2) XP_011520503.1:p.Pro22ArgfsTer10
NM_004212.4:c.65del (SLC28A2) MANE Select NP_004203.2:p.Pro22ArgfsTer10