Canonical Allele Identifier: CA594705547

Gene: SLC29A3

Linked Data

• dbSNP Id: rs1399066352
• gnomAD v2: 10-73122506-A-G
• gnomAD v3: 10-71362749-A-G
• gnomAD v4: 10-71362749-A-G
• MyVariant Identifiers: chr10:g.73122506A>G (hg19) ; chr10:g.71362749A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362749A>G , CM000672.2:g.71362749A>G	GRCh38
NC_000010.10:g.73122506A>G , CM000672.1:g.73122506A>G	GRCh37
NC_000010.9:g.72792512A>G	NCBI36
NG_017066.1:g.48497A>G
NG_017066.2:g.48491A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3045A>G
ENST00000373189.6:c.*141A>G MANE Select	ENSP00000362285.5:n.*141A>G
ENST00000479577.2:c.*141A>G	ENSP00000493995.1:n.*141A>G
ENST00000642198.1:c.*1141A>G	ENSP00000494827.1:n.*1141A>G
ENST00000642772.1:c.*94+6506A>G	ENSP00000495041.1:n.*94+6506A>G
ENST00000643042.1:c.1190A>G	ENSP00000496674.1:n.1190A>G
ENST00000643619.1:c.*1152A>G	ENSP00000494378.1:n.*1152A>G
ENST00000643752.1:c.*895A>G	ENSP00000495000.1:n.*895A>G
ENST00000644088.1:c.*890A>G	ENSP00000494066.1:n.*890A>G
ENST00000644591.1:c.*895A>G	ENSP00000496664.1:n.*895A>G
ENST00000644895.1:c.*99+6506A>G	ENSP00000493872.1:n.*99+6506A>G
ENST00000645345.1:c.*1141A>G	ENSP00000495859.1:n.*1141A>G
ENST00000647524.1:c.*1152A>G	ENSP00000495077.1:n.*1152A>G
ENST00000373189.5:c.*141A>G	ENSP00000362285.5:n.*141A>G
NM_001174098.1:c.*798A>G	NP_001167569.1:n.*798A>G
NM_018344.5:c.*141A>G	NP_060814.4:n.*141A>G
NR_033413.1:n.1543A>G
NR_033414.1:n.1316A>G
XM_006717910.2:c.*141A>G	XP_006717973.1:n.*141A>G
NM_001363518.1:c.*141A>G	NP_001350447.1:n.*141A>G
XM_017016377.2:c.*141A>G	XP_016871866.1:n.*141A>G
XM_017016378.2:c.*141A>G	XP_016871867.1:n.*141A>G
NM_018344.6:c.*141A>G MANE Select	NP_060814.4:n.*141A>G
NM_001174098.2:c.*798A>G	NP_001167569.1:n.*798A>G
NM_001363518.2:c.*141A>G	NP_001350447.1:n.*141A>G
NR_033413.2:n.1537A>G
NR_033414.2:n.1310A>G