Canonical Allele Identifier: CA470281634

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122278G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362521G>A , CM000672.2:g.71362521G>A	GRCh38
NC_000010.10:g.73122278G>A , CM000672.1:g.73122278G>A	GRCh37
NC_000010.9:g.72792284G>A	NCBI36
NG_017066.1:g.48269G>A
NG_017066.2:g.48263G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2817G>A
ENST00000373189.6:c.1341G>A MANE Select	ENSP00000362285.5:p.Glu447=
ENST00000479577.2:c.1107G>A	ENSP00000493995.1:p.Glu369=
ENST00000642198.1:c.*913G>A	ENSP00000494827.1:n.*913G>A
ENST00000642772.1:c.*94+6278G>A	ENSP00000495041.1:n.*94+6278G>A
ENST00000643042.1:c.962G>A	ENSP00000496674.1:n.962G>A
ENST00000643619.1:c.*924G>A	ENSP00000494378.1:n.*924G>A
ENST00000643752.1:c.*667G>A	ENSP00000495000.1:n.*667G>A
ENST00000644088.1:c.*662G>A	ENSP00000494066.1:n.*662G>A
ENST00000644591.1:c.*667G>A	ENSP00000496664.1:n.*667G>A
ENST00000644895.1:c.*99+6278G>A	ENSP00000493872.1:n.*99+6278G>A
ENST00000645345.1:c.*913G>A	ENSP00000495859.1:n.*913G>A
ENST00000647524.1:c.*924G>A	ENSP00000495077.1:n.*924G>A
ENST00000373189.5:c.1341G>A	ENSP00000362285.5:p.Glu447=
NM_001174098.1:c.*570G>A	NP_001167569.1:n.*570G>A
NM_018344.5:c.1341G>A	NP_060814.4:p.Glu447=
NR_033413.1:n.1315G>A
NR_033414.1:n.1088G>A
XM_006717910.2:c.1107G>A	XP_006717973.1:p.Glu369=
NM_001363518.1:c.1107G>A	NP_001350447.1:p.Glu369=
XM_017016377.2:c.903G>A	XP_016871866.1:p.Glu301=
XM_017016378.2:c.723G>A	XP_016871867.1:p.Glu241=
NM_018344.6:c.1341G>A MANE Select	NP_060814.4:p.Glu447=
NM_001174098.2:c.*570G>A	NP_001167569.1:n.*570G>A
NM_001363518.2:c.1107G>A	NP_001350447.1:p.Glu369=
NR_033413.2:n.1309G>A
NR_033414.2:n.1082G>A