Canonical Allele Identifier: CA470281307

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122095G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362338G>A , CM000672.2:g.71362338G>A	GRCh38
NC_000010.10:g.73122095G>A , CM000672.1:g.73122095G>A	GRCh37
NC_000010.9:g.72792101G>A	NCBI36
NG_017066.1:g.48086G>A
NG_017066.2:g.48080G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2634G>A
ENST00000373189.6:c.1158G>A MANE Select	ENSP00000362285.5:p.Arg386=
ENST00000479577.2:c.924G>A	ENSP00000493995.1:p.Arg308=
ENST00000642198.1:c.*730G>A	ENSP00000494827.1:n.*730G>A
ENST00000642772.1:c.*94+6095G>A	ENSP00000495041.1:n.*94+6095G>A
ENST00000643042.1:c.779G>A	ENSP00000496674.1:n.779G>A
ENST00000643619.1:c.*741G>A	ENSP00000494378.1:n.*741G>A
ENST00000643752.1:c.*484G>A	ENSP00000495000.1:n.*484G>A
ENST00000644088.1:c.*479G>A	ENSP00000494066.1:n.*479G>A
ENST00000644591.1:c.*484G>A	ENSP00000496664.1:n.*484G>A
ENST00000644895.1:c.*99+6095G>A	ENSP00000493872.1:n.*99+6095G>A
ENST00000645345.1:c.*730G>A	ENSP00000495859.1:n.*730G>A
ENST00000647524.1:c.*741G>A	ENSP00000495077.1:n.*741G>A
ENST00000373189.5:c.1158G>A	ENSP00000362285.5:p.Arg386=
ENST00000469204.1:n.655G>A
NM_001174098.1:c.*387G>A	NP_001167569.1:n.*387G>A
NM_018344.5:c.1158G>A	NP_060814.4:p.Arg386=
NR_033413.1:n.1132G>A
NR_033414.1:n.905G>A
XM_006717910.2:c.924G>A	XP_006717973.1:p.Arg308=
NM_001363518.1:c.924G>A	NP_001350447.1:p.Arg308=
XM_017016377.2:c.720G>A	XP_016871866.1:p.Arg240=
XM_017016378.2:c.540G>A	XP_016871867.1:p.Arg180=
NM_018344.6:c.1158G>A MANE Select	NP_060814.4:p.Arg386=
NM_001174098.2:c.*387G>A	NP_001167569.1:n.*387G>A
NM_001363518.2:c.924G>A	NP_001350447.1:p.Arg308=
NR_033413.2:n.1126G>A
NR_033414.2:n.899G>A