Canonical Allele Identifier: CA2609558730

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362727-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362727A>G , CM000672.2:g.71362727A>G	GRCh38
NC_000010.10:g.73122484A>G , CM000672.1:g.73122484A>G	GRCh37
NC_000010.9:g.72792490A>G	NCBI36
NG_017066.1:g.48475A>G
NG_017066.2:g.48469A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3023A>G
ENST00000373189.6:c.*119A>G MANE Select	ENSP00000362285.5:n.*119A>G
ENST00000479577.2:c.*119A>G	ENSP00000493995.1:n.*119A>G
ENST00000642198.1:c.*1119A>G	ENSP00000494827.1:n.*1119A>G
ENST00000642772.1:c.*94+6484A>G	ENSP00000495041.1:n.*94+6484A>G
ENST00000643042.1:c.1168A>G	ENSP00000496674.1:n.1168A>G
ENST00000643619.1:c.*1130A>G	ENSP00000494378.1:n.*1130A>G
ENST00000643752.1:c.*873A>G	ENSP00000495000.1:n.*873A>G
ENST00000644088.1:c.*868A>G	ENSP00000494066.1:n.*868A>G
ENST00000644591.1:c.*873A>G	ENSP00000496664.1:n.*873A>G
ENST00000644895.1:c.*99+6484A>G	ENSP00000493872.1:n.*99+6484A>G
ENST00000645345.1:c.*1119A>G	ENSP00000495859.1:n.*1119A>G
ENST00000647524.1:c.*1130A>G	ENSP00000495077.1:n.*1130A>G
ENST00000373189.5:c.*119A>G	ENSP00000362285.5:n.*119A>G
NM_001174098.1:c.*776A>G	NP_001167569.1:n.*776A>G
NM_018344.5:c.*119A>G	NP_060814.4:n.*119A>G
NR_033413.1:n.1521A>G
NR_033414.1:n.1294A>G
XM_006717910.2:c.*119A>G	XP_006717973.1:n.*119A>G
NM_001363518.1:c.*119A>G	NP_001350447.1:n.*119A>G
XM_017016377.2:c.*119A>G	XP_016871866.1:n.*119A>G
XM_017016378.2:c.*119A>G	XP_016871867.1:n.*119A>G
NM_018344.6:c.*119A>G MANE Select	NP_060814.4:n.*119A>G
NM_001174098.2:c.*776A>G	NP_001167569.1:n.*776A>G
NM_001363518.2:c.*119A>G	NP_001350447.1:n.*119A>G
NR_033413.2:n.1515A>G
NR_033414.2:n.1288A>G