Canonical Allele Identifier: CA470280797

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121750T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361993T>G , CM000672.2:g.71361993T>G	GRCh38
NC_000010.10:g.73121750T>G , CM000672.1:g.73121750T>G	GRCh37
NC_000010.9:g.72791756T>G	NCBI36
NG_017066.1:g.47741T>G
NG_017066.2:g.47735T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2289T>G
ENST00000373189.6:c.813T>G MANE Select	ENSP00000362285.5:p.Ser271=
ENST00000479577.2:c.579T>G	ENSP00000493995.1:p.Ser193=
ENST00000642198.1:c.*385T>G	ENSP00000494827.1:n.*385T>G
ENST00000642772.1:c.*94+5750T>G	ENSP00000495041.1:n.*94+5750T>G
ENST00000643042.1:c.434T>G	ENSP00000496674.1:n.434T>G
ENST00000643619.1:c.*396T>G	ENSP00000494378.1:n.*396T>G
ENST00000643752.1:c.*139T>G	ENSP00000495000.1:n.*139T>G
ENST00000644088.1:c.*134T>G	ENSP00000494066.1:n.*134T>G
ENST00000644591.1:c.*139T>G	ENSP00000496664.1:n.*139T>G
ENST00000644895.1:c.*99+5750T>G	ENSP00000493872.1:n.*99+5750T>G
ENST00000645345.1:c.*385T>G	ENSP00000495859.1:n.*385T>G
ENST00000647524.1:c.*396T>G	ENSP00000495077.1:n.*396T>G
ENST00000373189.5:c.813T>G	ENSP00000362285.5:p.Ser271=
ENST00000469204.1:n.310T>G
NM_001174098.1:c.*42T>G	NP_001167569.1:n.*42T>G
NM_018344.5:c.813T>G	NP_060814.4:p.Ser271=
NR_033413.1:n.787T>G
NR_033414.1:n.560T>G
XM_006717910.2:c.579T>G	XP_006717973.1:p.Ser193=
NM_001363518.1:c.579T>G	NP_001350447.1:p.Ser193=
XM_017016377.2:c.375T>G	XP_016871866.1:p.Ser125=
XM_017016378.2:c.195T>G	XP_016871867.1:p.Ser65=
NM_018344.6:c.813T>G MANE Select	NP_060814.4:p.Ser271=
NM_001174098.2:c.*42T>G	NP_001167569.1:n.*42T>G
NM_001363518.2:c.579T>G	NP_001350447.1:p.Ser193=
NR_033413.2:n.781T>G
NR_033414.2:n.554T>G