Canonical Allele Identifier: CA470280823

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121762G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362005G>A , CM000672.2:g.71362005G>A	GRCh38
NC_000010.10:g.73121762G>A , CM000672.1:g.73121762G>A	GRCh37
NC_000010.9:g.72791768G>A	NCBI36
NG_017066.1:g.47753G>A
NG_017066.2:g.47747G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2301G>A
ENST00000373189.6:c.825G>A MANE Select	ENSP00000362285.5:p.Glu275=
ENST00000479577.2:c.591G>A	ENSP00000493995.1:p.Glu197=
ENST00000642198.1:c.*397G>A	ENSP00000494827.1:n.*397G>A
ENST00000642772.1:c.*94+5762G>A	ENSP00000495041.1:n.*94+5762G>A
ENST00000643042.1:c.446G>A	ENSP00000496674.1:n.446G>A
ENST00000643619.1:c.*408G>A	ENSP00000494378.1:n.*408G>A
ENST00000643752.1:c.*151G>A	ENSP00000495000.1:n.*151G>A
ENST00000644088.1:c.*146G>A	ENSP00000494066.1:n.*146G>A
ENST00000644591.1:c.*151G>A	ENSP00000496664.1:n.*151G>A
ENST00000644895.1:c.*99+5762G>A	ENSP00000493872.1:n.*99+5762G>A
ENST00000645345.1:c.*397G>A	ENSP00000495859.1:n.*397G>A
ENST00000647524.1:c.*408G>A	ENSP00000495077.1:n.*408G>A
ENST00000373189.5:c.825G>A	ENSP00000362285.5:p.Glu275=
ENST00000469204.1:n.322G>A
NM_001174098.1:c.*54G>A	NP_001167569.1:n.*54G>A
NM_018344.5:c.825G>A	NP_060814.4:p.Glu275=
NR_033413.1:n.799G>A
NR_033414.1:n.572G>A
XM_006717910.2:c.591G>A	XP_006717973.1:p.Glu197=
NM_001363518.1:c.591G>A	NP_001350447.1:p.Glu197=
XM_017016377.2:c.387G>A	XP_016871866.1:p.Glu129=
XM_017016378.2:c.207G>A	XP_016871867.1:p.Glu69=
NM_018344.6:c.825G>A MANE Select	NP_060814.4:p.Glu275=
NM_001174098.2:c.*54G>A	NP_001167569.1:n.*54G>A
NM_001363518.2:c.591G>A	NP_001350447.1:p.Glu197=
NR_033413.2:n.793G>A
NR_033414.2:n.566G>A