Canonical Allele Identifier: CA2609558781

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362778-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362778T>G , CM000672.2:g.71362778T>G	GRCh38
NC_000010.10:g.73122535T>G , CM000672.1:g.73122535T>G	GRCh37
NC_000010.9:g.72792541T>G	NCBI36
NG_017066.1:g.48526T>G
NG_017066.2:g.48520T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3074T>G
ENST00000373189.6:c.*170T>G MANE Select	ENSP00000362285.5:n.*170T>G
ENST00000479577.2:c.*170T>G	ENSP00000493995.1:n.*170T>G
ENST00000642198.1:c.*1170T>G	ENSP00000494827.1:n.*1170T>G
ENST00000642772.1:c.*94+6535T>G	ENSP00000495041.1:n.*94+6535T>G
ENST00000643042.1:c.1219T>G	ENSP00000496674.1:n.1219T>G
ENST00000643619.1:c.*1181T>G	ENSP00000494378.1:n.*1181T>G
ENST00000643752.1:c.*924T>G	ENSP00000495000.1:n.*924T>G
ENST00000644088.1:c.*919T>G	ENSP00000494066.1:n.*919T>G
ENST00000644591.1:c.*924T>G	ENSP00000496664.1:n.*924T>G
ENST00000644895.1:c.*99+6535T>G	ENSP00000493872.1:n.*99+6535T>G
ENST00000645345.1:c.*1170T>G	ENSP00000495859.1:n.*1170T>G
ENST00000647524.1:c.*1181T>G	ENSP00000495077.1:n.*1181T>G
ENST00000373189.5:c.*170T>G	ENSP00000362285.5:n.*170T>G
NM_001174098.1:c.*827T>G	NP_001167569.1:n.*827T>G
NM_018344.5:c.*170T>G	NP_060814.4:n.*170T>G
NR_033413.1:n.1572T>G
NR_033414.1:n.1345T>G
XM_006717910.2:c.*170T>G	XP_006717973.1:n.*170T>G
NM_001363518.1:c.*170T>G	NP_001350447.1:n.*170T>G
XM_017016377.2:c.*170T>G	XP_016871866.1:n.*170T>G
XM_017016378.2:c.*170T>G	XP_016871867.1:n.*170T>G
NM_018344.6:c.*170T>G MANE Select	NP_060814.4:n.*170T>G
NM_001174098.2:c.*827T>G	NP_001167569.1:n.*827T>G
NM_001363518.2:c.*170T>G	NP_001350447.1:n.*170T>G
NR_033413.2:n.1566T>G
NR_033414.2:n.1339T>G