Canonical Allele Identifier: CA209387865
Gene: SLC29A3 HGNC NCBI

Linked Data

dbSNP Id: rs756965136

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71362117_71362125del , CM000672.2:g.71362117_71362125del GRCh38
NC_000010.10:g.73121874_73121882del , CM000672.1:g.73121874_73121882del GRCh37
NC_000010.9:g.72791880_72791888del NCBI36
NG_017066.1:g.47865_47873del
NG_017066.2:g.47859_47867del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697843.1:n.2413_2421del
ENST00000373189.6:c.937_945del MANE Select ENSP00000362285.5:p.Thr313_Val315del
ENST00000479577.2:c.703_711del ENSP00000493995.1:p.Thr235_Val237del
ENST00000642198.1:c.*509_*517del ENSP00000494827.1:n.*509_*517del
ENST00000642772.1:c.*94+5874_*94+5882del ENSP00000495041.1:n.*94+5874_*94+5882del
ENST00000643042.1:c.558_566del ENSP00000496674.1:n.558_566del
ENST00000643619.1:c.*520_*528del ENSP00000494378.1:n.*520_*528del
ENST00000643752.1:c.*263_*271del ENSP00000495000.1:n.*263_*271del
ENST00000644088.1:c.*258_*266del ENSP00000494066.1:n.*258_*266del
ENST00000644591.1:c.*263_*271del ENSP00000496664.1:n.*263_*271del
ENST00000644895.1:c.*99+5874_*99+5882del ENSP00000493872.1:n.*99+5874_*99+5882del
ENST00000645345.1:c.*509_*517del ENSP00000495859.1:n.*509_*517del
ENST00000647524.1:c.*520_*528del ENSP00000495077.1:n.*520_*528del
ENST00000373189.5:c.937_945del ENSP00000362285.5:p.Thr313_Val315del
ENST00000469204.1:n.434_442del
NM_001174098.1:c.*166_*174del NP_001167569.1:n.*166_*174del
NM_018344.5:c.937_945del NP_060814.4:p.Thr313_Val315del
NR_033413.1:n.911_919del
NR_033414.1:n.684_692del
XM_006717910.2:c.703_711del XP_006717973.1:p.Thr235_Val237del
NM_001363518.1:c.703_711del NP_001350447.1:p.Thr235_Val237del
XM_017016377.2:c.499_507del XP_016871866.1:p.Thr167_Val169del
XM_017016378.2:c.319_327del XP_016871867.1:p.Thr107_Val109del
NM_018344.6:c.937_945del MANE Select NP_060814.4:p.Thr313_Val315del
NM_001174098.2:c.*166_*174del NP_001167569.1:n.*166_*174del
NM_001363518.2:c.703_711del NP_001350447.1:p.Thr235_Val237del
NR_033413.2:n.905_913del
NR_033414.2:n.678_686del