Canonical Allele Identifier: CA1918678652

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362749A= , CM000672.2:g.71362749A=	GRCh38
NC_000010.10:g.73122506A= , CM000672.1:g.73122506A=	GRCh37
NC_000010.9:g.72792512A=	NCBI36
NG_017066.1:g.48497A=
NG_017066.2:g.48491A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3045A=
ENST00000373189.6:c.*141A= MANE Select	ENSP00000362285.5:n.*141A=
ENST00000479577.2:c.*141A=	ENSP00000493995.1:n.*141A=
ENST00000642198.1:c.*1141A=	ENSP00000494827.1:n.*1141A=
ENST00000642772.1:c.*94+6506A=	ENSP00000495041.1:n.*94+6506A=
ENST00000643042.1:c.1190A=	ENSP00000496674.1:n.1190A=
ENST00000643619.1:c.*1152A=	ENSP00000494378.1:n.*1152A=
ENST00000643752.1:c.*895A=	ENSP00000495000.1:n.*895A=
ENST00000644088.1:c.*890A=	ENSP00000494066.1:n.*890A=
ENST00000644591.1:c.*895A=	ENSP00000496664.1:n.*895A=
ENST00000644895.1:c.*99+6506A=	ENSP00000493872.1:n.*99+6506A=
ENST00000645345.1:c.*1141A=	ENSP00000495859.1:n.*1141A=
ENST00000647524.1:c.*1152A=	ENSP00000495077.1:n.*1152A=
ENST00000373189.5:c.*141A=	ENSP00000362285.5:n.*141A=
NM_001174098.1:c.*798A=	NP_001167569.1:n.*798A=
NM_018344.5:c.*141A=	NP_060814.4:n.*141A=
NR_033413.1:n.1543A=
NR_033414.1:n.1316A=
XM_006717910.2:c.*141A=	XP_006717973.1:n.*141A=
NM_001363518.1:c.*141A=	NP_001350447.1:n.*141A=
XM_017016377.2:c.*141A=	XP_016871866.1:n.*141A=
XM_017016378.2:c.*141A=	XP_016871867.1:n.*141A=
NM_018344.6:c.*141A= MANE Select	NP_060814.4:n.*141A=
NM_001174098.2:c.*798A=	NP_001167569.1:n.*798A=
NM_001363518.2:c.*141A=	NP_001350447.1:n.*141A=
NR_033413.2:n.1537A=
NR_033414.2:n.1310A=