Canonical Allele Identifier: CA2609558708

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362696-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362696T>A , CM000672.2:g.71362696T>A	GRCh38
NC_000010.10:g.73122453T>A , CM000672.1:g.73122453T>A	GRCh37
NC_000010.9:g.72792459T>A	NCBI36
NG_017066.1:g.48444T>A
NG_017066.2:g.48438T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2992T>A
ENST00000373189.6:c.*88T>A MANE Select	ENSP00000362285.5:n.*88T>A
ENST00000479577.2:c.*88T>A	ENSP00000493995.1:n.*88T>A
ENST00000642198.1:c.*1088T>A	ENSP00000494827.1:n.*1088T>A
ENST00000642772.1:c.*94+6453T>A	ENSP00000495041.1:n.*94+6453T>A
ENST00000643042.1:c.1137T>A	ENSP00000496674.1:n.1137T>A
ENST00000643619.1:c.*1099T>A	ENSP00000494378.1:n.*1099T>A
ENST00000643752.1:c.*842T>A	ENSP00000495000.1:n.*842T>A
ENST00000644088.1:c.*837T>A	ENSP00000494066.1:n.*837T>A
ENST00000644591.1:c.*842T>A	ENSP00000496664.1:n.*842T>A
ENST00000644895.1:c.*99+6453T>A	ENSP00000493872.1:n.*99+6453T>A
ENST00000645345.1:c.*1088T>A	ENSP00000495859.1:n.*1088T>A
ENST00000647524.1:c.*1099T>A	ENSP00000495077.1:n.*1099T>A
ENST00000373189.5:c.*88T>A	ENSP00000362285.5:n.*88T>A
NM_001174098.1:c.*745T>A	NP_001167569.1:n.*745T>A
NM_018344.5:c.*88T>A	NP_060814.4:n.*88T>A
NR_033413.1:n.1490T>A
NR_033414.1:n.1263T>A
XM_006717910.2:c.*88T>A	XP_006717973.1:n.*88T>A
NM_001363518.1:c.*88T>A	NP_001350447.1:n.*88T>A
XM_017016377.2:c.*88T>A	XP_016871866.1:n.*88T>A
XM_017016378.2:c.*88T>A	XP_016871867.1:n.*88T>A
NM_018344.6:c.*88T>A MANE Select	NP_060814.4:n.*88T>A
NM_001174098.2:c.*745T>A	NP_001167569.1:n.*745T>A
NM_001363518.2:c.*88T>A	NP_001350447.1:n.*88T>A
NR_033413.2:n.1484T>A
NR_033414.2:n.1257T>A