Canonical Allele Identifier: CA470280811

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121756A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361999A>G , CM000672.2:g.71361999A>G	GRCh38
NC_000010.10:g.73121756A>G , CM000672.1:g.73121756A>G	GRCh37
NC_000010.9:g.72791762A>G	NCBI36
NG_017066.1:g.47747A>G
NG_017066.2:g.47741A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2295A>G
ENST00000373189.6:c.819A>G MANE Select	ENSP00000362285.5:p.Glu273=
ENST00000479577.2:c.585A>G	ENSP00000493995.1:p.Glu195=
ENST00000642198.1:c.*391A>G	ENSP00000494827.1:n.*391A>G
ENST00000642772.1:c.*94+5756A>G	ENSP00000495041.1:n.*94+5756A>G
ENST00000643042.1:c.440A>G	ENSP00000496674.1:n.440A>G
ENST00000643619.1:c.*402A>G	ENSP00000494378.1:n.*402A>G
ENST00000643752.1:c.*145A>G	ENSP00000495000.1:n.*145A>G
ENST00000644088.1:c.*140A>G	ENSP00000494066.1:n.*140A>G
ENST00000644591.1:c.*145A>G	ENSP00000496664.1:n.*145A>G
ENST00000644895.1:c.*99+5756A>G	ENSP00000493872.1:n.*99+5756A>G
ENST00000645345.1:c.*391A>G	ENSP00000495859.1:n.*391A>G
ENST00000647524.1:c.*402A>G	ENSP00000495077.1:n.*402A>G
ENST00000373189.5:c.819A>G	ENSP00000362285.5:p.Glu273=
ENST00000469204.1:n.316A>G
NM_001174098.1:c.*48A>G	NP_001167569.1:n.*48A>G
NM_018344.5:c.819A>G	NP_060814.4:p.Glu273=
NR_033413.1:n.793A>G
NR_033414.1:n.566A>G
XM_006717910.2:c.585A>G	XP_006717973.1:p.Glu195=
NM_001363518.1:c.585A>G	NP_001350447.1:p.Glu195=
XM_017016377.2:c.381A>G	XP_016871866.1:p.Glu127=
XM_017016378.2:c.201A>G	XP_016871867.1:p.Glu67=
NM_018344.6:c.819A>G MANE Select	NP_060814.4:p.Glu273=
NM_001174098.2:c.*48A>G	NP_001167569.1:n.*48A>G
NM_001363518.2:c.585A>G	NP_001350447.1:p.Glu195=
NR_033413.2:n.787A>G
NR_033414.2:n.560A>G