Canonical Allele Identifier: CA1918678357
Gene: SLC29A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71362119_71362120delinsCT , CM000672.2:g.71362119_71362120delinsCT GRCh38
NC_000010.10:g.73121876_73121877delinsCT , CM000672.1:g.73121876_73121877delinsCT GRCh37
NC_000010.9:g.72791882_72791883delinsCT NCBI36
NG_017066.1:g.47867_47868delinsCT
NG_017066.2:g.47861_47862delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000697843.1:n.2415_2416delinsCT
ENST00000373189.6:c.939_940delinsCT MANE Select ENSP00000362285.5:p.Thr313=
ENST00000479577.2:c.705_706delinsCT ENSP00000493995.1:p.Thr235=
ENST00000642198.1:c.*511_*512delinsCT ENSP00000494827.1:n.*511_*512delinsCT
ENST00000642772.1:c.*94+5876_*94+5877delinsCT ENSP00000495041.1:n.*94+5876_*94+5877delinsCT
ENST00000643042.1:c.560_561delinsCT ENSP00000496674.1:n.560_561delinsCT
ENST00000643619.1:c.*522_*523delinsCT ENSP00000494378.1:n.*522_*523delinsCT
ENST00000643752.1:c.*265_*266delinsCT ENSP00000495000.1:n.*265_*266delinsCT
ENST00000644088.1:c.*260_*261delinsCT ENSP00000494066.1:n.*260_*261delinsCT
ENST00000644591.1:c.*265_*266delinsCT ENSP00000496664.1:n.*265_*266delinsCT
ENST00000644895.1:c.*99+5876_*99+5877delinsCT ENSP00000493872.1:n.*99+5876_*99+5877delinsCT
ENST00000645345.1:c.*511_*512delinsCT ENSP00000495859.1:n.*511_*512delinsCT
ENST00000647524.1:c.*522_*523delinsCT ENSP00000495077.1:n.*522_*523delinsCT
ENST00000373189.5:c.939_940delinsCT ENSP00000362285.5:p.Thr313=
ENST00000469204.1:n.436_437delinsCT
NM_001174098.1:c.*168_*169delinsCT NP_001167569.1:n.*168_*169delinsCT
NM_018344.5:c.939_940delinsCT NP_060814.4:p.Thr313=
NR_033413.1:n.913_914delinsCT
NR_033414.1:n.686_687delinsCT
XM_006717910.2:c.705_706delinsCT XP_006717973.1:p.Thr235=
NM_001363518.1:c.705_706delinsCT NP_001350447.1:p.Thr235=
XM_017016377.2:c.501_502delinsCT XP_016871866.1:p.Thr167=
XM_017016378.2:c.321_322delinsCT XP_016871867.1:p.Thr107=
NM_018344.6:c.939_940delinsCT MANE Select NP_060814.4:p.Thr313=
NM_001174098.2:c.*168_*169delinsCT NP_001167569.1:n.*168_*169delinsCT
NM_001363518.2:c.705_706delinsCT NP_001350447.1:p.Thr235=
NR_033413.2:n.907_908delinsCT
NR_033414.2:n.680_681delinsCT