Canonical Allele Identifier: CA1918678439
Gene: SLC29A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71362302C= , CM000672.2:g.71362302C= GRCh38
NC_000010.10:g.73122059C= , CM000672.1:g.73122059C= GRCh37
NC_000010.9:g.72792065C= NCBI36
NG_017066.1:g.48050C=
NG_017066.2:g.48044C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697843.1:n.2598C=
ENST00000373189.6:c.1122C= MANE Select ENSP00000362285.5:p.Pro374=
ENST00000479577.2:c.888C= ENSP00000493995.1:p.Pro296=
ENST00000642198.1:c.*694C= ENSP00000494827.1:n.*694C=
ENST00000642772.1:c.*94+6059C= ENSP00000495041.1:n.*94+6059C=
ENST00000643042.1:c.743C= ENSP00000496674.1:n.743C=
ENST00000643619.1:c.*705C= ENSP00000494378.1:n.*705C=
ENST00000643752.1:c.*448C= ENSP00000495000.1:n.*448C=
ENST00000644088.1:c.*443C= ENSP00000494066.1:n.*443C=
ENST00000644591.1:c.*448C= ENSP00000496664.1:n.*448C=
ENST00000644895.1:c.*99+6059C= ENSP00000493872.1:n.*99+6059C=
ENST00000645345.1:c.*694C= ENSP00000495859.1:n.*694C=
ENST00000647524.1:c.*705C= ENSP00000495077.1:n.*705C=
ENST00000373189.5:c.1122C= ENSP00000362285.5:p.Pro374=
ENST00000469204.1:n.619C=
NM_001174098.1:c.*351C= NP_001167569.1:n.*351C=
NM_018344.5:c.1122C= NP_060814.4:p.Pro374=
NR_033413.1:n.1096C=
NR_033414.1:n.869C=
XM_006717910.2:c.888C= XP_006717973.1:p.Pro296=
NM_001363518.1:c.888C= NP_001350447.1:p.Pro296=
XM_017016377.2:c.684C= XP_016871866.1:p.Pro228=
XM_017016378.2:c.504C= XP_016871867.1:p.Pro168=
NM_018344.6:c.1122C= MANE Select NP_060814.4:p.Pro374=
NM_001174098.2:c.*351C= NP_001167569.1:n.*351C=
NM_001363518.2:c.888C= NP_001350447.1:p.Pro296=
NR_033413.2:n.1090C=
NR_033414.2:n.863C=