Canonical Allele Identifier: CA2609558761

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362758-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362758G>A , CM000672.2:g.71362758G>A	GRCh38
NC_000010.10:g.73122515G>A , CM000672.1:g.73122515G>A	GRCh37
NC_000010.9:g.72792521G>A	NCBI36
NG_017066.1:g.48506G>A
NG_017066.2:g.48500G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3054G>A
ENST00000373189.6:c.*150G>A MANE Select	ENSP00000362285.5:n.*150G>A
ENST00000479577.2:c.*150G>A	ENSP00000493995.1:n.*150G>A
ENST00000642198.1:c.*1150G>A	ENSP00000494827.1:n.*1150G>A
ENST00000642772.1:c.*94+6515G>A	ENSP00000495041.1:n.*94+6515G>A
ENST00000643042.1:c.1199G>A	ENSP00000496674.1:n.1199G>A
ENST00000643619.1:c.*1161G>A	ENSP00000494378.1:n.*1161G>A
ENST00000643752.1:c.*904G>A	ENSP00000495000.1:n.*904G>A
ENST00000644088.1:c.*899G>A	ENSP00000494066.1:n.*899G>A
ENST00000644591.1:c.*904G>A	ENSP00000496664.1:n.*904G>A
ENST00000644895.1:c.*99+6515G>A	ENSP00000493872.1:n.*99+6515G>A
ENST00000645345.1:c.*1150G>A	ENSP00000495859.1:n.*1150G>A
ENST00000647524.1:c.*1161G>A	ENSP00000495077.1:n.*1161G>A
ENST00000373189.5:c.*150G>A	ENSP00000362285.5:n.*150G>A
NM_001174098.1:c.*807G>A	NP_001167569.1:n.*807G>A
NM_018344.5:c.*150G>A	NP_060814.4:n.*150G>A
NR_033413.1:n.1552G>A
NR_033414.1:n.1325G>A
XM_006717910.2:c.*150G>A	XP_006717973.1:n.*150G>A
NM_001363518.1:c.*150G>A	NP_001350447.1:n.*150G>A
XM_017016377.2:c.*150G>A	XP_016871866.1:n.*150G>A
XM_017016378.2:c.*150G>A	XP_016871867.1:n.*150G>A
NM_018344.6:c.*150G>A MANE Select	NP_060814.4:n.*150G>A
NM_001174098.2:c.*807G>A	NP_001167569.1:n.*807G>A
NM_001363518.2:c.*150G>A	NP_001350447.1:n.*150G>A
NR_033413.2:n.1546G>A
NR_033414.2:n.1319G>A