Canonical Allele Identifier: CA1918678327

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362065A= , CM000672.2:g.71362065A=	GRCh38
NC_000010.10:g.73121822A= , CM000672.1:g.73121822A=	GRCh37
NC_000010.9:g.72791828A=	NCBI36
NG_017066.1:g.47813A=
NG_017066.2:g.47807A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2361A=
ENST00000373189.6:c.885A= MANE Select	ENSP00000362285.5:p.Thr295=
ENST00000479577.2:c.651A=	ENSP00000493995.1:p.Thr217=
ENST00000642198.1:c.*457A=	ENSP00000494827.1:n.*457A=
ENST00000642772.1:c.*94+5822A=	ENSP00000495041.1:n.*94+5822A=
ENST00000643042.1:c.506A=	ENSP00000496674.1:n.506A=
ENST00000643619.1:c.*468A=	ENSP00000494378.1:n.*468A=
ENST00000643752.1:c.*211A=	ENSP00000495000.1:n.*211A=
ENST00000644088.1:c.*206A=	ENSP00000494066.1:n.*206A=
ENST00000644591.1:c.*211A=	ENSP00000496664.1:n.*211A=
ENST00000644895.1:c.*99+5822A=	ENSP00000493872.1:n.*99+5822A=
ENST00000645345.1:c.*457A=	ENSP00000495859.1:n.*457A=
ENST00000647524.1:c.*468A=	ENSP00000495077.1:n.*468A=
ENST00000373189.5:c.885A=	ENSP00000362285.5:p.Thr295=
ENST00000469204.1:n.382A=
NM_001174098.1:c.*114A=	NP_001167569.1:n.*114A=
NM_018344.5:c.885A=	NP_060814.4:p.Thr295=
NR_033413.1:n.859A=
NR_033414.1:n.632A=
XM_006717910.2:c.651A=	XP_006717973.1:p.Thr217=
NM_001363518.1:c.651A=	NP_001350447.1:p.Thr217=
XM_017016377.2:c.447A=	XP_016871866.1:p.Thr149=
XM_017016378.2:c.267A=	XP_016871867.1:p.Thr89=
NM_018344.6:c.885A= MANE Select	NP_060814.4:p.Thr295=
NM_001174098.2:c.*114A=	NP_001167569.1:n.*114A=
NM_001363518.2:c.651A=	NP_001350447.1:p.Thr217=
NR_033413.2:n.853A=
NR_033414.2:n.626A=