Canonical Allele Identifier: CA1918678396
Gene: SLC29A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71362190C= , CM000672.2:g.71362190C= GRCh38
NC_000010.10:g.73121947C= , CM000672.1:g.73121947C= GRCh37
NC_000010.9:g.72791953C= NCBI36
NG_017066.1:g.47938C=
NG_017066.2:g.47932C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697843.1:n.2486C=
ENST00000373189.6:c.1010C= MANE Select ENSP00000362285.5:p.Ser337=
ENST00000479577.2:c.776C= ENSP00000493995.1:p.Ser259=
ENST00000642198.1:c.*582C= ENSP00000494827.1:n.*582C=
ENST00000642772.1:c.*94+5947C= ENSP00000495041.1:n.*94+5947C=
ENST00000643042.1:c.631C= ENSP00000496674.1:n.631C=
ENST00000643619.1:c.*593C= ENSP00000494378.1:n.*593C=
ENST00000643752.1:c.*336C= ENSP00000495000.1:n.*336C=
ENST00000644088.1:c.*331C= ENSP00000494066.1:n.*331C=
ENST00000644591.1:c.*336C= ENSP00000496664.1:n.*336C=
ENST00000644895.1:c.*99+5947C= ENSP00000493872.1:n.*99+5947C=
ENST00000645345.1:c.*582C= ENSP00000495859.1:n.*582C=
ENST00000647524.1:c.*593C= ENSP00000495077.1:n.*593C=
ENST00000373189.5:c.1010C= ENSP00000362285.5:p.Ser337=
ENST00000469204.1:n.507C=
NM_001174098.1:c.*239C= NP_001167569.1:n.*239C=
NM_018344.5:c.1010C= NP_060814.4:p.Ser337=
NR_033413.1:n.984C=
NR_033414.1:n.757C=
XM_006717910.2:c.776C= XP_006717973.1:p.Ser259=
NM_001363518.1:c.776C= NP_001350447.1:p.Ser259=
XM_017016377.2:c.572C= XP_016871866.1:p.Ser191=
XM_017016378.2:c.392C= XP_016871867.1:p.Ser131=
NM_018344.6:c.1010C= MANE Select NP_060814.4:p.Ser337=
NM_001174098.2:c.*239C= NP_001167569.1:n.*239C=
NM_001363518.2:c.776C= NP_001350447.1:p.Ser259=
NR_033413.2:n.978C=
NR_033414.2:n.751C=