Canonical Allele Identifier: CA2609558754

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362748-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362748C>A , CM000672.2:g.71362748C>A	GRCh38
NC_000010.10:g.73122505C>A , CM000672.1:g.73122505C>A	GRCh37
NC_000010.9:g.72792511C>A	NCBI36
NG_017066.1:g.48496C>A
NG_017066.2:g.48490C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3044C>A
ENST00000373189.6:c.*140C>A MANE Select	ENSP00000362285.5:n.*140C>A
ENST00000479577.2:c.*140C>A	ENSP00000493995.1:n.*140C>A
ENST00000642198.1:c.*1140C>A	ENSP00000494827.1:n.*1140C>A
ENST00000642772.1:c.*94+6505C>A	ENSP00000495041.1:n.*94+6505C>A
ENST00000643042.1:c.1189C>A	ENSP00000496674.1:n.1189C>A
ENST00000643619.1:c.*1151C>A	ENSP00000494378.1:n.*1151C>A
ENST00000643752.1:c.*894C>A	ENSP00000495000.1:n.*894C>A
ENST00000644088.1:c.*889C>A	ENSP00000494066.1:n.*889C>A
ENST00000644591.1:c.*894C>A	ENSP00000496664.1:n.*894C>A
ENST00000644895.1:c.*99+6505C>A	ENSP00000493872.1:n.*99+6505C>A
ENST00000645345.1:c.*1140C>A	ENSP00000495859.1:n.*1140C>A
ENST00000647524.1:c.*1151C>A	ENSP00000495077.1:n.*1151C>A
ENST00000373189.5:c.*140C>A	ENSP00000362285.5:n.*140C>A
NM_001174098.1:c.*797C>A	NP_001167569.1:n.*797C>A
NM_018344.5:c.*140C>A	NP_060814.4:n.*140C>A
NR_033413.1:n.1542C>A
NR_033414.1:n.1315C>A
XM_006717910.2:c.*140C>A	XP_006717973.1:n.*140C>A
NM_001363518.1:c.*140C>A	NP_001350447.1:n.*140C>A
XM_017016377.2:c.*140C>A	XP_016871866.1:n.*140C>A
XM_017016378.2:c.*140C>A	XP_016871867.1:n.*140C>A
NM_018344.6:c.*140C>A MANE Select	NP_060814.4:n.*140C>A
NM_001174098.2:c.*797C>A	NP_001167569.1:n.*797C>A
NM_001363518.2:c.*140C>A	NP_001350447.1:n.*140C>A
NR_033413.2:n.1536C>A
NR_033414.2:n.1309C>A