Canonical Allele Identifier: CA470281036

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121849G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362092G>A , CM000672.2:g.71362092G>A	GRCh38
NC_000010.10:g.73121849G>A , CM000672.1:g.73121849G>A	GRCh37
NC_000010.9:g.72791855G>A	NCBI36
NG_017066.1:g.47840G>A
NG_017066.2:g.47834G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2388G>A
ENST00000373189.6:c.912G>A MANE Select	ENSP00000362285.5:p.Lys304=
ENST00000479577.2:c.678G>A	ENSP00000493995.1:p.Lys226=
ENST00000642198.1:c.*484G>A	ENSP00000494827.1:n.*484G>A
ENST00000642772.1:c.*94+5849G>A	ENSP00000495041.1:n.*94+5849G>A
ENST00000643042.1:c.533G>A	ENSP00000496674.1:n.533G>A
ENST00000643619.1:c.*495G>A	ENSP00000494378.1:n.*495G>A
ENST00000643752.1:c.*238G>A	ENSP00000495000.1:n.*238G>A
ENST00000644088.1:c.*233G>A	ENSP00000494066.1:n.*233G>A
ENST00000644591.1:c.*238G>A	ENSP00000496664.1:n.*238G>A
ENST00000644895.1:c.*99+5849G>A	ENSP00000493872.1:n.*99+5849G>A
ENST00000645345.1:c.*484G>A	ENSP00000495859.1:n.*484G>A
ENST00000647524.1:c.*495G>A	ENSP00000495077.1:n.*495G>A
ENST00000373189.5:c.912G>A	ENSP00000362285.5:p.Lys304=
ENST00000469204.1:n.409G>A
NM_001174098.1:c.*141G>A	NP_001167569.1:n.*141G>A
NM_018344.5:c.912G>A	NP_060814.4:p.Lys304=
NR_033413.1:n.886G>A
NR_033414.1:n.659G>A
XM_006717910.2:c.678G>A	XP_006717973.1:p.Lys226=
NM_001363518.1:c.678G>A	NP_001350447.1:p.Lys226=
XM_017016377.2:c.474G>A	XP_016871866.1:p.Lys158=
XM_017016378.2:c.294G>A	XP_016871867.1:p.Lys98=
NM_018344.6:c.912G>A MANE Select	NP_060814.4:p.Lys304=
NM_001174098.2:c.*141G>A	NP_001167569.1:n.*141G>A
NM_001363518.2:c.678G>A	NP_001350447.1:p.Lys226=
NR_033413.2:n.880G>A
NR_033414.2:n.653G>A