Canonical Allele Identifier: CA377114173

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121783T>A (hg19) ; chr10:g.71362026T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362026T>A , CM000672.2:g.71362026T>A	GRCh38
NC_000010.10:g.73121783T>A , CM000672.1:g.73121783T>A	GRCh37
NC_000010.9:g.72791789T>A	NCBI36
NG_017066.1:g.47774T>A
NG_017066.2:g.47768T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2322T>A
ENST00000373189.6:c.846T>A MANE Select	ENSP00000362285.5:p.Ser282Arg
ENST00000479577.2:c.612T>A	ENSP00000493995.1:p.Ser204Arg
ENST00000642198.1:c.*418T>A	ENSP00000494827.1:n.*418T>A
ENST00000642772.1:c.*94+5783T>A	ENSP00000495041.1:n.*94+5783T>A
ENST00000643042.1:c.467T>A	ENSP00000496674.1:n.467T>A
ENST00000643619.1:c.*429T>A	ENSP00000494378.1:n.*429T>A
ENST00000643752.1:c.*172T>A	ENSP00000495000.1:n.*172T>A
ENST00000644088.1:c.*167T>A	ENSP00000494066.1:n.*167T>A
ENST00000644591.1:c.*172T>A	ENSP00000496664.1:n.*172T>A
ENST00000644895.1:c.*99+5783T>A	ENSP00000493872.1:n.*99+5783T>A
ENST00000645345.1:c.*418T>A	ENSP00000495859.1:n.*418T>A
ENST00000647524.1:c.*429T>A	ENSP00000495077.1:n.*429T>A
ENST00000373189.5:c.846T>A	ENSP00000362285.5:p.Ser282Arg
ENST00000469204.1:n.343T>A
NM_001174098.1:c.*75T>A	NP_001167569.1:n.*75T>A
NM_018344.5:c.846T>A	NP_060814.4:p.Ser282Arg
NR_033413.1:n.820T>A
NR_033414.1:n.593T>A
XM_006717910.2:c.612T>A	XP_006717973.1:p.Ser204Arg
NM_001363518.1:c.612T>A	NP_001350447.1:p.Ser204Arg
XM_017016377.2:c.408T>A	XP_016871866.1:p.Ser136Arg
XM_017016378.2:c.228T>A	XP_016871867.1:p.Ser76Arg
NM_018344.6:c.846T>A MANE Select	NP_060814.4:p.Ser282Arg
NM_001174098.2:c.*75T>A	NP_001167569.1:n.*75T>A
NM_001363518.2:c.612T>A	NP_001350447.1:p.Ser204Arg
NR_033413.2:n.814T>A
NR_033414.2:n.587T>A