Canonical Allele Identifier: CA1918678593

Gene: SLC29A3

Linked Data

• dbSNP Id: rs1847098427
• gnomAD v4: 10-71362627-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362627A>G , CM000672.2:g.71362627A>G	GRCh38
NC_000010.10:g.73122384A>G , CM000672.1:g.73122384A>G	GRCh37
NC_000010.9:g.72792390A>G	NCBI36
NG_017066.1:g.48375A>G
NG_017066.2:g.48369A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2923A>G
ENST00000373189.6:c.*19A>G MANE Select	ENSP00000362285.5:n.*19A>G
ENST00000479577.2:c.*19A>G	ENSP00000493995.1:n.*19A>G
ENST00000642198.1:c.*1019A>G	ENSP00000494827.1:n.*1019A>G
ENST00000642772.1:c.*94+6384A>G	ENSP00000495041.1:n.*94+6384A>G
ENST00000643042.1:c.1068A>G	ENSP00000496674.1:n.1068A>G
ENST00000643619.1:c.*1030A>G	ENSP00000494378.1:n.*1030A>G
ENST00000643752.1:c.*773A>G	ENSP00000495000.1:n.*773A>G
ENST00000644088.1:c.*768A>G	ENSP00000494066.1:n.*768A>G
ENST00000644591.1:c.*773A>G	ENSP00000496664.1:n.*773A>G
ENST00000644895.1:c.*99+6384A>G	ENSP00000493872.1:n.*99+6384A>G
ENST00000645345.1:c.*1019A>G	ENSP00000495859.1:n.*1019A>G
ENST00000647524.1:c.*1030A>G	ENSP00000495077.1:n.*1030A>G
ENST00000373189.5:c.*19A>G	ENSP00000362285.5:n.*19A>G
NM_001174098.1:c.*676A>G	NP_001167569.1:n.*676A>G
NM_018344.5:c.*19A>G	NP_060814.4:n.*19A>G
NR_033413.1:n.1421A>G
NR_033414.1:n.1194A>G
XM_006717910.2:c.*19A>G	XP_006717973.1:n.*19A>G
NM_001363518.1:c.*19A>G	NP_001350447.1:n.*19A>G
XM_017016377.2:c.*19A>G	XP_016871866.1:n.*19A>G
XM_017016378.2:c.*19A>G	XP_016871867.1:n.*19A>G
NM_018344.6:c.*19A>G MANE Select	NP_060814.4:n.*19A>G
NM_001174098.2:c.*676A>G	NP_001167569.1:n.*676A>G
NM_001363518.2:c.*19A>G	NP_001350447.1:n.*19A>G
NR_033413.2:n.1415A>G
NR_033414.2:n.1188A>G