Canonical Allele Identifier: CA377116565

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362282-T-G
• MyVariant Identifiers: chr10:g.73122039T>G (hg19) ; chr10:g.71362282T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362282T>G , CM000672.2:g.71362282T>G	GRCh38
NC_000010.10:g.73122039T>G , CM000672.1:g.73122039T>G	GRCh37
NC_000010.9:g.72792045T>G	NCBI36
NG_017066.1:g.48030T>G
NG_017066.2:g.48024T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2578T>G
ENST00000373189.6:c.1102T>G MANE Select	ENSP00000362285.5:p.Trp368Gly
ENST00000479577.2:c.868T>G	ENSP00000493995.1:p.Trp290Gly
ENST00000642198.1:c.*674T>G	ENSP00000494827.1:n.*674T>G
ENST00000642772.1:c.*94+6039T>G	ENSP00000495041.1:n.*94+6039T>G
ENST00000643042.1:c.723T>G	ENSP00000496674.1:n.723T>G
ENST00000643619.1:c.*685T>G	ENSP00000494378.1:n.*685T>G
ENST00000643752.1:c.*428T>G	ENSP00000495000.1:n.*428T>G
ENST00000644088.1:c.*423T>G	ENSP00000494066.1:n.*423T>G
ENST00000644591.1:c.*428T>G	ENSP00000496664.1:n.*428T>G
ENST00000644895.1:c.*99+6039T>G	ENSP00000493872.1:n.*99+6039T>G
ENST00000645345.1:c.*674T>G	ENSP00000495859.1:n.*674T>G
ENST00000647524.1:c.*685T>G	ENSP00000495077.1:n.*685T>G
ENST00000373189.5:c.1102T>G	ENSP00000362285.5:p.Trp368Gly
ENST00000469204.1:n.599T>G
NM_001174098.1:c.*331T>G	NP_001167569.1:n.*331T>G
NM_018344.5:c.1102T>G	NP_060814.4:p.Trp368Gly
NR_033413.1:n.1076T>G
NR_033414.1:n.849T>G
XM_006717910.2:c.868T>G	XP_006717973.1:p.Trp290Gly
NM_001363518.1:c.868T>G	NP_001350447.1:p.Trp290Gly
XM_017016377.2:c.664T>G	XP_016871866.1:p.Trp222Gly
XM_017016378.2:c.484T>G	XP_016871867.1:p.Trp162Gly
NM_018344.6:c.1102T>G MANE Select	NP_060814.4:p.Trp368Gly
NM_001174098.2:c.*331T>G	NP_001167569.1:n.*331T>G
NM_001363518.2:c.868T>G	NP_001350447.1:p.Trp290Gly
NR_033413.2:n.1070T>G
NR_033414.2:n.843T>G