Canonical Allele Identifier: CA2609558666

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362304-ATAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362305_71362307del , CM000672.2:g.71362305_71362307del	GRCh38
NC_000010.10:g.73122062_73122064del , CM000672.1:g.73122062_73122064del	GRCh37
NC_000010.9:g.72792068_72792070del	NCBI36
NG_017066.1:g.48053_48055del
NG_017066.2:g.48047_48049del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2601_2603del
ENST00000373189.6:c.1125_1127del MANE Select	ENSP00000362285.5:p.Ser376del
ENST00000479577.2:c.891_893del	ENSP00000493995.1:p.Ser298del
ENST00000642198.1:c.*697_*699del	ENSP00000494827.1:n.*697_*699del
ENST00000642772.1:c.*94+6062_*94+6064del	ENSP00000495041.1:n.*94+6062_*94+6064del
ENST00000643042.1:c.746_748del	ENSP00000496674.1:n.746_748del
ENST00000643619.1:c.*708_*710del	ENSP00000494378.1:n.*708_*710del
ENST00000643752.1:c.*451_*453del	ENSP00000495000.1:n.*451_*453del
ENST00000644088.1:c.*446_*448del	ENSP00000494066.1:n.*446_*448del
ENST00000644591.1:c.*451_*453del	ENSP00000496664.1:n.*451_*453del
ENST00000644895.1:c.*99+6062_*99+6064del	ENSP00000493872.1:n.*99+6062_*99+6064del
ENST00000645345.1:c.*697_*699del	ENSP00000495859.1:n.*697_*699del
ENST00000647524.1:c.*708_*710del	ENSP00000495077.1:n.*708_*710del
ENST00000373189.5:c.1125_1127del	ENSP00000362285.5:p.Ser376del
ENST00000469204.1:n.622_624del
NM_001174098.1:c.*354_*356del	NP_001167569.1:n.*354_*356del
NM_018344.5:c.1125_1127del	NP_060814.4:p.Ser376del
NR_033413.1:n.1099_1101del
NR_033414.1:n.872_874del
XM_006717910.2:c.891_893del	XP_006717973.1:p.Ser298del
NM_001363518.1:c.891_893del	NP_001350447.1:p.Ser298del
XM_017016377.2:c.687_689del	XP_016871866.1:p.Ser230del
XM_017016378.2:c.507_509del	XP_016871867.1:p.Ser170del
NM_018344.6:c.1125_1127del MANE Select	NP_060814.4:p.Ser376del
NM_001174098.2:c.*354_*356del	NP_001167569.1:n.*354_*356del
NM_001363518.2:c.891_893del	NP_001350447.1:p.Ser298del
NR_033413.2:n.1093_1095del
NR_033414.2:n.866_868del