Canonical Allele Identifier: CA1918678289

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361978G= , CM000672.2:g.71361978G=	GRCh38
NC_000010.10:g.73121735G= , CM000672.1:g.73121735G=	GRCh37
NC_000010.9:g.72791741G=	NCBI36
NG_017066.1:g.47726G=
NG_017066.2:g.47720G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2274G=
ENST00000373189.6:c.798G= MANE Select	ENSP00000362285.5:p.Ala266=
ENST00000479577.2:c.564G=	ENSP00000493995.1:p.Ala188=
ENST00000642198.1:c.*370G=	ENSP00000494827.1:n.*370G=
ENST00000642772.1:c.*94+5735G=	ENSP00000495041.1:n.*94+5735G=
ENST00000643042.1:c.419G=	ENSP00000496674.1:n.419G=
ENST00000643619.1:c.*381G=	ENSP00000494378.1:n.*381G=
ENST00000643752.1:c.*124G=	ENSP00000495000.1:n.*124G=
ENST00000644088.1:c.*119G=	ENSP00000494066.1:n.*119G=
ENST00000644591.1:c.*124G=	ENSP00000496664.1:n.*124G=
ENST00000644895.1:c.*99+5735G=	ENSP00000493872.1:n.*99+5735G=
ENST00000645345.1:c.*370G=	ENSP00000495859.1:n.*370G=
ENST00000647524.1:c.*381G=	ENSP00000495077.1:n.*381G=
ENST00000373189.5:c.798G=	ENSP00000362285.5:p.Ala266=
ENST00000469204.1:n.295G=
NM_001174098.1:c.*27G=	NP_001167569.1:n.*27G=
NM_018344.5:c.798G=	NP_060814.4:p.Ala266=
NR_033413.1:n.772G=
NR_033414.1:n.545G=
XM_006717910.2:c.564G=	XP_006717973.1:p.Ala188=
NM_001363518.1:c.564G=	NP_001350447.1:p.Ala188=
XM_017016377.2:c.360G=	XP_016871866.1:p.Ala120=
XM_017016378.2:c.180G=	XP_016871867.1:p.Ala60=
NM_018344.6:c.798G= MANE Select	NP_060814.4:p.Ala266=
NM_001174098.2:c.*27G=	NP_001167569.1:n.*27G=
NM_001363518.2:c.564G=	NP_001350447.1:p.Ala188=
NR_033413.2:n.766G=
NR_033414.2:n.539G=