Canonical Allele Identifier: CA2609558778

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362773-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362776del , CM000672.2:g.71362776del	GRCh38
NC_000010.10:g.73122533del , CM000672.1:g.73122533del	GRCh37
NC_000010.9:g.72792539del	NCBI36
NG_017066.1:g.48524del
NG_017066.2:g.48518del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3072del
ENST00000373189.6:c.*168del MANE Select	ENSP00000362285.5:n.*168del
ENST00000479577.2:c.*168del	ENSP00000493995.1:n.*168del
ENST00000642198.1:c.*1168del	ENSP00000494827.1:n.*1168del
ENST00000642772.1:c.*94+6533del	ENSP00000495041.1:n.*94+6533del
ENST00000643042.1:c.1217del	ENSP00000496674.1:n.1217del
ENST00000643619.1:c.*1179del	ENSP00000494378.1:n.*1179del
ENST00000643752.1:c.*922del	ENSP00000495000.1:n.*922del
ENST00000644088.1:c.*917del	ENSP00000494066.1:n.*917del
ENST00000644591.1:c.*922del	ENSP00000496664.1:n.*922del
ENST00000644895.1:c.*99+6533del	ENSP00000493872.1:n.*99+6533del
ENST00000645345.1:c.*1168del	ENSP00000495859.1:n.*1168del
ENST00000647524.1:c.*1179del	ENSP00000495077.1:n.*1179del
ENST00000373189.5:c.*168del	ENSP00000362285.5:n.*168del
NM_001174098.1:c.*825del	NP_001167569.1:n.*825del
NM_018344.5:c.*168del	NP_060814.4:n.*168del
NR_033413.1:n.1570del
NR_033414.1:n.1343del
XM_006717910.2:c.*168del	XP_006717973.1:n.*168del
NM_001363518.1:c.*168del	NP_001350447.1:n.*168del
XM_017016377.2:c.*168del	XP_016871866.1:n.*168del
XM_017016378.2:c.*168del	XP_016871867.1:n.*168del
NM_018344.6:c.*168del MANE Select	NP_060814.4:n.*168del
NM_001174098.2:c.*825del	NP_001167569.1:n.*825del
NM_001363518.2:c.*168del	NP_001350447.1:n.*168del
NR_033413.2:n.1564del
NR_033414.2:n.1337del