Canonical Allele Identifier: CA1918678649

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362739C= , CM000672.2:g.71362739C=	GRCh38
NC_000010.10:g.73122496C= , CM000672.1:g.73122496C=	GRCh37
NC_000010.9:g.72792502C=	NCBI36
NG_017066.1:g.48487C=
NG_017066.2:g.48481C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3035C=
ENST00000373189.6:c.*131C= MANE Select	ENSP00000362285.5:n.*131C=
ENST00000479577.2:c.*131C=	ENSP00000493995.1:n.*131C=
ENST00000642198.1:c.*1131C=	ENSP00000494827.1:n.*1131C=
ENST00000642772.1:c.*94+6496C=	ENSP00000495041.1:n.*94+6496C=
ENST00000643042.1:c.1180C=	ENSP00000496674.1:n.1180C=
ENST00000643619.1:c.*1142C=	ENSP00000494378.1:n.*1142C=
ENST00000643752.1:c.*885C=	ENSP00000495000.1:n.*885C=
ENST00000644088.1:c.*880C=	ENSP00000494066.1:n.*880C=
ENST00000644591.1:c.*885C=	ENSP00000496664.1:n.*885C=
ENST00000644895.1:c.*99+6496C=	ENSP00000493872.1:n.*99+6496C=
ENST00000645345.1:c.*1131C=	ENSP00000495859.1:n.*1131C=
ENST00000647524.1:c.*1142C=	ENSP00000495077.1:n.*1142C=
ENST00000373189.5:c.*131C=	ENSP00000362285.5:n.*131C=
NM_001174098.1:c.*788C=	NP_001167569.1:n.*788C=
NM_018344.5:c.*131C=	NP_060814.4:n.*131C=
NR_033413.1:n.1533C=
NR_033414.1:n.1306C=
XM_006717910.2:c.*131C=	XP_006717973.1:n.*131C=
NM_001363518.1:c.*131C=	NP_001350447.1:n.*131C=
XM_017016377.2:c.*131C=	XP_016871866.1:n.*131C=
XM_017016378.2:c.*131C=	XP_016871867.1:n.*131C=
NM_018344.6:c.*131C= MANE Select	NP_060814.4:n.*131C=
NM_001174098.2:c.*788C=	NP_001167569.1:n.*788C=
NM_001363518.2:c.*131C=	NP_001350447.1:n.*131C=
NR_033413.2:n.1527C=
NR_033414.2:n.1300C=