Canonical Allele Identifier: CA377114743

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121851C>A (hg19) ; chr10:g.71362094C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362094C>A , CM000672.2:g.71362094C>A	GRCh38
NC_000010.10:g.73121851C>A , CM000672.1:g.73121851C>A	GRCh37
NC_000010.9:g.72791857C>A	NCBI36
NG_017066.1:g.47842C>A
NG_017066.2:g.47836C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2390C>A
ENST00000373189.6:c.914C>A MANE Select	ENSP00000362285.5:p.Thr305Lys
ENST00000479577.2:c.680C>A	ENSP00000493995.1:p.Thr227Lys
ENST00000642198.1:c.*486C>A	ENSP00000494827.1:n.*486C>A
ENST00000642772.1:c.*94+5851C>A	ENSP00000495041.1:n.*94+5851C>A
ENST00000643042.1:c.535C>A	ENSP00000496674.1:n.535C>A
ENST00000643619.1:c.*497C>A	ENSP00000494378.1:n.*497C>A
ENST00000643752.1:c.*240C>A	ENSP00000495000.1:n.*240C>A
ENST00000644088.1:c.*235C>A	ENSP00000494066.1:n.*235C>A
ENST00000644591.1:c.*240C>A	ENSP00000496664.1:n.*240C>A
ENST00000644895.1:c.*99+5851C>A	ENSP00000493872.1:n.*99+5851C>A
ENST00000645345.1:c.*486C>A	ENSP00000495859.1:n.*486C>A
ENST00000647524.1:c.*497C>A	ENSP00000495077.1:n.*497C>A
ENST00000373189.5:c.914C>A	ENSP00000362285.5:p.Thr305Lys
ENST00000469204.1:n.411C>A
NM_001174098.1:c.*143C>A	NP_001167569.1:n.*143C>A
NM_018344.5:c.914C>A	NP_060814.4:p.Thr305Lys
NR_033413.1:n.888C>A
NR_033414.1:n.661C>A
XM_006717910.2:c.680C>A	XP_006717973.1:p.Thr227Lys
NM_001363518.1:c.680C>A	NP_001350447.1:p.Thr227Lys
XM_017016377.2:c.476C>A	XP_016871866.1:p.Thr159Lys
XM_017016378.2:c.296C>A	XP_016871867.1:p.Thr99Lys
NM_018344.6:c.914C>A MANE Select	NP_060814.4:p.Thr305Lys
NM_001174098.2:c.*143C>A	NP_001167569.1:n.*143C>A
NM_001363518.2:c.680C>A	NP_001350447.1:p.Thr227Lys
NR_033413.2:n.882C>A
NR_033414.2:n.655C>A