Canonical Allele Identifier: CA5543057

Gene: SLC29A3

Linked Data

• ClinVar Variation Id: 300364
• ClinVar RCV Id: RCV000365829
• dbSNP Id: rs142991278
• ExAC: 10:73121734 C / T
• gnomAD v2: 10-73121734-C-T
• gnomAD v3: 10-71361977-C-T
• gnomAD v4: 10-71361977-C-T
• MyVariant Identifiers: chr10:g.73121734C>T (hg19) ; chr10:g.71361977C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361977C>T , CM000672.2:g.71361977C>T	GRCh38
NC_000010.10:g.73121734C>T , CM000672.1:g.73121734C>T	GRCh37
NC_000010.9:g.72791740C>T	NCBI36
NG_017066.1:g.47725C>T
NG_017066.2:g.47719C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2273C>T
ENST00000373189.6:c.797C>T MANE Select	ENSP00000362285.5:p.Ala266Val
ENST00000479577.2:c.563C>T	ENSP00000493995.1:p.Ala188Val
ENST00000642198.1:c.*369C>T	ENSP00000494827.1:n.*369C>T
ENST00000642772.1:c.*94+5734C>T	ENSP00000495041.1:n.*94+5734C>T
ENST00000643042.1:c.418C>T	ENSP00000496674.1:n.418C>T
ENST00000643619.1:c.*380C>T	ENSP00000494378.1:n.*380C>T
ENST00000643752.1:c.*123C>T	ENSP00000495000.1:n.*123C>T
ENST00000644088.1:c.*118C>T	ENSP00000494066.1:n.*118C>T
ENST00000644591.1:c.*123C>T	ENSP00000496664.1:n.*123C>T
ENST00000644895.1:c.*99+5734C>T	ENSP00000493872.1:n.*99+5734C>T
ENST00000645345.1:c.*369C>T	ENSP00000495859.1:n.*369C>T
ENST00000647524.1:c.*380C>T	ENSP00000495077.1:n.*380C>T
ENST00000373189.5:c.797C>T	ENSP00000362285.5:p.Ala266Val
ENST00000469204.1:n.294C>T
NM_001174098.1:c.*26C>T	NP_001167569.1:n.*26C>T
NM_018344.5:c.797C>T	NP_060814.4:p.Ala266Val
NR_033413.1:n.771C>T
NR_033414.1:n.544C>T
XM_006717910.2:c.563C>T	XP_006717973.1:p.Ala188Val
NM_001363518.1:c.563C>T	NP_001350447.1:p.Ala188Val
XM_017016377.2:c.359C>T	XP_016871866.1:p.Ala120Val
XM_017016378.2:c.179C>T	XP_016871867.1:p.Ala60Val
NM_018344.6:c.797C>T MANE Select	NP_060814.4:p.Ala266Val
NM_001174098.2:c.*26C>T	NP_001167569.1:n.*26C>T
NM_001363518.2:c.563C>T	NP_001350447.1:p.Ala188Val
NR_033413.2:n.765C>T
NR_033414.2:n.538C>T