Canonical Allele Identifier: CA1918678386

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362173G= , CM000672.2:g.71362173G=	GRCh38
NC_000010.10:g.73121930G= , CM000672.1:g.73121930G=	GRCh37
NC_000010.9:g.72791936G=	NCBI36
NG_017066.1:g.47921G=
NG_017066.2:g.47915G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2469G=
ENST00000373189.6:c.993G= MANE Select	ENSP00000362285.5:p.Glu331=
ENST00000479577.2:c.759G=	ENSP00000493995.1:p.Glu253=
ENST00000642198.1:c.*565G=	ENSP00000494827.1:n.*565G=
ENST00000642772.1:c.*94+5930G=	ENSP00000495041.1:n.*94+5930G=
ENST00000643042.1:c.614G=	ENSP00000496674.1:n.614G=
ENST00000643619.1:c.*576G=	ENSP00000494378.1:n.*576G=
ENST00000643752.1:c.*319G=	ENSP00000495000.1:n.*319G=
ENST00000644088.1:c.*314G=	ENSP00000494066.1:n.*314G=
ENST00000644591.1:c.*319G=	ENSP00000496664.1:n.*319G=
ENST00000644895.1:c.*99+5930G=	ENSP00000493872.1:n.*99+5930G=
ENST00000645345.1:c.*565G=	ENSP00000495859.1:n.*565G=
ENST00000647524.1:c.*576G=	ENSP00000495077.1:n.*576G=
ENST00000373189.5:c.993G=	ENSP00000362285.5:p.Glu331=
ENST00000469204.1:n.490G=
NM_001174098.1:c.*222G=	NP_001167569.1:n.*222G=
NM_018344.5:c.993G=	NP_060814.4:p.Glu331=
NR_033413.1:n.967G=
NR_033414.1:n.740G=
XM_006717910.2:c.759G=	XP_006717973.1:p.Glu253=
NM_001363518.1:c.759G=	NP_001350447.1:p.Glu253=
XM_017016377.2:c.555G=	XP_016871866.1:p.Glu185=
XM_017016378.2:c.375G=	XP_016871867.1:p.Glu125=
NM_018344.6:c.993G= MANE Select	NP_060814.4:p.Glu331=
NM_001174098.2:c.*222G=	NP_001167569.1:n.*222G=
NM_001363518.2:c.759G=	NP_001350447.1:p.Glu253=
NR_033413.2:n.961G=
NR_033414.2:n.734G=