Canonical Allele Identifier: CA1918678363
Gene: SLC29A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71362138A= , CM000672.2:g.71362138A= GRCh38
NC_000010.10:g.73121895A= , CM000672.1:g.73121895A= GRCh37
NC_000010.9:g.72791901A= NCBI36
NG_017066.1:g.47886A=
NG_017066.2:g.47880A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697843.1:n.2434A=
ENST00000373189.6:c.958A= MANE Select ENSP00000362285.5:p.Ser320=
ENST00000479577.2:c.724A= ENSP00000493995.1:p.Ser242=
ENST00000642198.1:c.*530A= ENSP00000494827.1:n.*530A=
ENST00000642772.1:c.*94+5895A= ENSP00000495041.1:n.*94+5895A=
ENST00000643042.1:c.579A= ENSP00000496674.1:n.579A=
ENST00000643619.1:c.*541A= ENSP00000494378.1:n.*541A=
ENST00000643752.1:c.*284A= ENSP00000495000.1:n.*284A=
ENST00000644088.1:c.*279A= ENSP00000494066.1:n.*279A=
ENST00000644591.1:c.*284A= ENSP00000496664.1:n.*284A=
ENST00000644895.1:c.*99+5895A= ENSP00000493872.1:n.*99+5895A=
ENST00000645345.1:c.*530A= ENSP00000495859.1:n.*530A=
ENST00000647524.1:c.*541A= ENSP00000495077.1:n.*541A=
ENST00000373189.5:c.958A= ENSP00000362285.5:p.Ser320=
ENST00000469204.1:n.455A=
NM_001174098.1:c.*187A= NP_001167569.1:n.*187A=
NM_018344.5:c.958A= NP_060814.4:p.Ser320=
NR_033413.1:n.932A=
NR_033414.1:n.705A=
XM_006717910.2:c.724A= XP_006717973.1:p.Ser242=
NM_001363518.1:c.724A= NP_001350447.1:p.Ser242=
XM_017016377.2:c.520A= XP_016871866.1:p.Ser174=
XM_017016378.2:c.340A= XP_016871867.1:p.Ser114=
NM_018344.6:c.958A= MANE Select NP_060814.4:p.Ser320=
NM_001174098.2:c.*187A= NP_001167569.1:n.*187A=
NM_001363518.2:c.724A= NP_001350447.1:p.Ser242=
NR_033413.2:n.926A=
NR_033414.2:n.699A=