Canonical Allele Identifier: CA470281618

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122269G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362512G>A , CM000672.2:g.71362512G>A	GRCh38
NC_000010.10:g.73122269G>A , CM000672.1:g.73122269G>A	GRCh37
NC_000010.9:g.72792275G>A	NCBI36
NG_017066.1:g.48260G>A
NG_017066.2:g.48254G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2808G>A
ENST00000373189.6:c.1332G>A MANE Select	ENSP00000362285.5:p.Glu444=
ENST00000479577.2:c.1098G>A	ENSP00000493995.1:p.Glu366=
ENST00000642198.1:c.*904G>A	ENSP00000494827.1:n.*904G>A
ENST00000642772.1:c.*94+6269G>A	ENSP00000495041.1:n.*94+6269G>A
ENST00000643042.1:c.953G>A	ENSP00000496674.1:n.953G>A
ENST00000643619.1:c.*915G>A	ENSP00000494378.1:n.*915G>A
ENST00000643752.1:c.*658G>A	ENSP00000495000.1:n.*658G>A
ENST00000644088.1:c.*653G>A	ENSP00000494066.1:n.*653G>A
ENST00000644591.1:c.*658G>A	ENSP00000496664.1:n.*658G>A
ENST00000644895.1:c.*99+6269G>A	ENSP00000493872.1:n.*99+6269G>A
ENST00000645345.1:c.*904G>A	ENSP00000495859.1:n.*904G>A
ENST00000647524.1:c.*915G>A	ENSP00000495077.1:n.*915G>A
ENST00000373189.5:c.1332G>A	ENSP00000362285.5:p.Glu444=
ENST00000469204.1:n.829G>A
NM_001174098.1:c.*561G>A	NP_001167569.1:n.*561G>A
NM_018344.5:c.1332G>A	NP_060814.4:p.Glu444=
NR_033413.1:n.1306G>A
NR_033414.1:n.1079G>A
XM_006717910.2:c.1098G>A	XP_006717973.1:p.Glu366=
NM_001363518.1:c.1098G>A	NP_001350447.1:p.Glu366=
XM_017016377.2:c.894G>A	XP_016871866.1:p.Glu298=
XM_017016378.2:c.714G>A	XP_016871867.1:p.Glu238=
NM_018344.6:c.1332G>A MANE Select	NP_060814.4:p.Glu444=
NM_001174098.2:c.*561G>A	NP_001167569.1:n.*561G>A
NM_001363518.2:c.1098G>A	NP_001350447.1:p.Glu366=
NR_033413.2:n.1300G>A
NR_033414.2:n.1073G>A