Canonical Allele Identifier: CA2609558782

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362779-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362779T>C , CM000672.2:g.71362779T>C	GRCh38
NC_000010.10:g.73122536T>C , CM000672.1:g.73122536T>C	GRCh37
NC_000010.9:g.72792542T>C	NCBI36
NG_017066.1:g.48527T>C
NG_017066.2:g.48521T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3075T>C
ENST00000373189.6:c.*171T>C MANE Select	ENSP00000362285.5:n.*171T>C
ENST00000479577.2:c.*171T>C	ENSP00000493995.1:n.*171T>C
ENST00000642198.1:c.*1171T>C	ENSP00000494827.1:n.*1171T>C
ENST00000642772.1:c.*94+6536T>C	ENSP00000495041.1:n.*94+6536T>C
ENST00000643042.1:c.1220T>C	ENSP00000496674.1:n.1220T>C
ENST00000643619.1:c.*1182T>C	ENSP00000494378.1:n.*1182T>C
ENST00000643752.1:c.*925T>C	ENSP00000495000.1:n.*925T>C
ENST00000644088.1:c.*920T>C	ENSP00000494066.1:n.*920T>C
ENST00000644591.1:c.*925T>C	ENSP00000496664.1:n.*925T>C
ENST00000644895.1:c.*99+6536T>C	ENSP00000493872.1:n.*99+6536T>C
ENST00000645345.1:c.*1171T>C	ENSP00000495859.1:n.*1171T>C
ENST00000647524.1:c.*1182T>C	ENSP00000495077.1:n.*1182T>C
ENST00000373189.5:c.*171T>C	ENSP00000362285.5:n.*171T>C
NM_001174098.1:c.*828T>C	NP_001167569.1:n.*828T>C
NM_018344.5:c.*171T>C	NP_060814.4:n.*171T>C
NR_033413.1:n.1573T>C
NR_033414.1:n.1346T>C
XM_006717910.2:c.*171T>C	XP_006717973.1:n.*171T>C
NM_001363518.1:c.*171T>C	NP_001350447.1:n.*171T>C
XM_017016377.2:c.*171T>C	XP_016871866.1:n.*171T>C
XM_017016378.2:c.*171T>C	XP_016871867.1:n.*171T>C
NM_018344.6:c.*171T>C MANE Select	NP_060814.4:n.*171T>C
NM_001174098.2:c.*828T>C	NP_001167569.1:n.*828T>C
NM_001363518.2:c.*171T>C	NP_001350447.1:n.*171T>C
NR_033413.2:n.1567T>C
NR_033414.2:n.1340T>C