Canonical Allele Identifier: CA2609558765

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362761-AGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362762_71362763del , CM000672.2:g.71362762_71362763del	GRCh38
NC_000010.10:g.73122519_73122520del , CM000672.1:g.73122519_73122520del	GRCh37
NC_000010.9:g.72792525_72792526del	NCBI36
NG_017066.1:g.48510_48511del
NG_017066.2:g.48504_48505del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3058_3059del
ENST00000373189.6:c.*154_*155del MANE Select	ENSP00000362285.5:n.*154_*155del
ENST00000479577.2:c.*154_*155del	ENSP00000493995.1:n.*154_*155del
ENST00000642198.1:c.*1154_*1155del	ENSP00000494827.1:n.*1154_*1155del
ENST00000642772.1:c.*94+6519_*94+6520del	ENSP00000495041.1:n.*94+6519_*94+6520del
ENST00000643042.1:c.1203_1204del	ENSP00000496674.1:n.1203_1204del
ENST00000643619.1:c.*1165_*1166del	ENSP00000494378.1:n.*1165_*1166del
ENST00000643752.1:c.*908_*909del	ENSP00000495000.1:n.*908_*909del
ENST00000644088.1:c.*903_*904del	ENSP00000494066.1:n.*903_*904del
ENST00000644591.1:c.*908_*909del	ENSP00000496664.1:n.*908_*909del
ENST00000644895.1:c.*99+6519_*99+6520del	ENSP00000493872.1:n.*99+6519_*99+6520del
ENST00000645345.1:c.*1154_*1155del	ENSP00000495859.1:n.*1154_*1155del
ENST00000647524.1:c.*1165_*1166del	ENSP00000495077.1:n.*1165_*1166del
ENST00000373189.5:c.*154_*155del	ENSP00000362285.5:n.*154_*155del
NM_001174098.1:c.*811_*812del	NP_001167569.1:n.*811_*812del
NM_018344.5:c.*154_*155del	NP_060814.4:n.*154_*155del
NR_033413.1:n.1556_1557del
NR_033414.1:n.1329_1330del
XM_006717910.2:c.*154_*155del	XP_006717973.1:n.*154_*155del
NM_001363518.1:c.*154_*155del	NP_001350447.1:n.*154_*155del
XM_017016377.2:c.*154_*155del	XP_016871866.1:n.*154_*155del
XM_017016378.2:c.*154_*155del	XP_016871867.1:n.*154_*155del
NM_018344.6:c.*154_*155del MANE Select	NP_060814.4:n.*154_*155del
NM_001174098.2:c.*811_*812del	NP_001167569.1:n.*811_*812del
NM_001363518.2:c.*154_*155del	NP_001350447.1:n.*154_*155del
NR_033413.2:n.1550_1551del
NR_033414.2:n.1323_1324del