Canonical Allele Identifier: CA1918678300
Gene: SLC29A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71362011C= , CM000672.2:g.71362011C= GRCh38
NC_000010.10:g.73121768C= , CM000672.1:g.73121768C= GRCh37
NC_000010.9:g.72791774C= NCBI36
NG_017066.1:g.47759C=
NG_017066.2:g.47753C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697843.1:n.2307C=
ENST00000373189.6:c.831C= MANE Select ENSP00000362285.5:p.Pro277=
ENST00000479577.2:c.597C= ENSP00000493995.1:p.Pro199=
ENST00000642198.1:c.*403C= ENSP00000494827.1:n.*403C=
ENST00000642772.1:c.*94+5768C= ENSP00000495041.1:n.*94+5768C=
ENST00000643042.1:c.452C= ENSP00000496674.1:n.452C=
ENST00000643619.1:c.*414C= ENSP00000494378.1:n.*414C=
ENST00000643752.1:c.*157C= ENSP00000495000.1:n.*157C=
ENST00000644088.1:c.*152C= ENSP00000494066.1:n.*152C=
ENST00000644591.1:c.*157C= ENSP00000496664.1:n.*157C=
ENST00000644895.1:c.*99+5768C= ENSP00000493872.1:n.*99+5768C=
ENST00000645345.1:c.*403C= ENSP00000495859.1:n.*403C=
ENST00000647524.1:c.*414C= ENSP00000495077.1:n.*414C=
ENST00000373189.5:c.831C= ENSP00000362285.5:p.Pro277=
ENST00000469204.1:n.328C=
NM_001174098.1:c.*60C= NP_001167569.1:n.*60C=
NM_018344.5:c.831C= NP_060814.4:p.Pro277=
NR_033413.1:n.805C=
NR_033414.1:n.578C=
XM_006717910.2:c.597C= XP_006717973.1:p.Pro199=
NM_001363518.1:c.597C= NP_001350447.1:p.Pro199=
XM_017016377.2:c.393C= XP_016871866.1:p.Pro131=
XM_017016378.2:c.213C= XP_016871867.1:p.Pro71=
NM_018344.6:c.831C= MANE Select NP_060814.4:p.Pro277=
NM_001174098.2:c.*60C= NP_001167569.1:n.*60C=
NM_001363518.2:c.597C= NP_001350447.1:p.Pro199=
NR_033413.2:n.799C=
NR_033414.2:n.572C=