Canonical Allele Identifier: CA594705553

Gene: SLC29A3

Linked Data

• dbSNP Id: rs1226823000
• gnomAD v2: 10-73122531-C-A
• gnomAD v3: 10-71362774-C-A
• gnomAD v4: 10-71362774-C-A
• MyVariant Identifiers: chr10:g.73122531C>A (hg19) ; chr10:g.71362774C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362774C>A , CM000672.2:g.71362774C>A	GRCh38
NC_000010.10:g.73122531C>A , CM000672.1:g.73122531C>A	GRCh37
NC_000010.9:g.72792537C>A	NCBI36
NG_017066.1:g.48522C>A
NG_017066.2:g.48516C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3070C>A
ENST00000373189.6:c.*166C>A MANE Select	ENSP00000362285.5:n.*166C>A
ENST00000479577.2:c.*166C>A	ENSP00000493995.1:n.*166C>A
ENST00000642198.1:c.*1166C>A	ENSP00000494827.1:n.*1166C>A
ENST00000642772.1:c.*94+6531C>A	ENSP00000495041.1:n.*94+6531C>A
ENST00000643042.1:c.1215C>A	ENSP00000496674.1:n.1215C>A
ENST00000643619.1:c.*1177C>A	ENSP00000494378.1:n.*1177C>A
ENST00000643752.1:c.*920C>A	ENSP00000495000.1:n.*920C>A
ENST00000644088.1:c.*915C>A	ENSP00000494066.1:n.*915C>A
ENST00000644591.1:c.*920C>A	ENSP00000496664.1:n.*920C>A
ENST00000644895.1:c.*99+6531C>A	ENSP00000493872.1:n.*99+6531C>A
ENST00000645345.1:c.*1166C>A	ENSP00000495859.1:n.*1166C>A
ENST00000647524.1:c.*1177C>A	ENSP00000495077.1:n.*1177C>A
ENST00000373189.5:c.*166C>A	ENSP00000362285.5:n.*166C>A
NM_001174098.1:c.*823C>A	NP_001167569.1:n.*823C>A
NM_018344.5:c.*166C>A	NP_060814.4:n.*166C>A
NR_033413.1:n.1568C>A
NR_033414.1:n.1341C>A
XM_006717910.2:c.*166C>A	XP_006717973.1:n.*166C>A
NM_001363518.1:c.*166C>A	NP_001350447.1:n.*166C>A
XM_017016377.2:c.*166C>A	XP_016871866.1:n.*166C>A
XM_017016378.2:c.*166C>A	XP_016871867.1:n.*166C>A
NM_018344.6:c.*166C>A MANE Select	NP_060814.4:n.*166C>A
NM_001174098.2:c.*823C>A	NP_001167569.1:n.*823C>A
NM_001363518.2:c.*166C>A	NP_001350447.1:n.*166C>A
NR_033413.2:n.1562C>A
NR_033414.2:n.1335C>A