Canonical Allele Identifier: CA1918678663

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362769C= , CM000672.2:g.71362769C=	GRCh38
NC_000010.10:g.73122526C= , CM000672.1:g.73122526C=	GRCh37
NC_000010.9:g.72792532C=	NCBI36
NG_017066.1:g.48517C=
NG_017066.2:g.48511C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.3065C=
ENST00000373189.6:c.*161C= MANE Select	ENSP00000362285.5:n.*161C=
ENST00000479577.2:c.*161C=	ENSP00000493995.1:n.*161C=
ENST00000642198.1:c.*1161C=	ENSP00000494827.1:n.*1161C=
ENST00000642772.1:c.*94+6526C=	ENSP00000495041.1:n.*94+6526C=
ENST00000643042.1:c.1210C=	ENSP00000496674.1:n.1210C=
ENST00000643619.1:c.*1172C=	ENSP00000494378.1:n.*1172C=
ENST00000643752.1:c.*915C=	ENSP00000495000.1:n.*915C=
ENST00000644088.1:c.*910C=	ENSP00000494066.1:n.*910C=
ENST00000644591.1:c.*915C=	ENSP00000496664.1:n.*915C=
ENST00000644895.1:c.*99+6526C=	ENSP00000493872.1:n.*99+6526C=
ENST00000645345.1:c.*1161C=	ENSP00000495859.1:n.*1161C=
ENST00000647524.1:c.*1172C=	ENSP00000495077.1:n.*1172C=
ENST00000373189.5:c.*161C=	ENSP00000362285.5:n.*161C=
NM_001174098.1:c.*818C=	NP_001167569.1:n.*818C=
NM_018344.5:c.*161C=	NP_060814.4:n.*161C=
NR_033413.1:n.1563C=
NR_033414.1:n.1336C=
XM_006717910.2:c.*161C=	XP_006717973.1:n.*161C=
NM_001363518.1:c.*161C=	NP_001350447.1:n.*161C=
XM_017016377.2:c.*161C=	XP_016871866.1:n.*161C=
XM_017016378.2:c.*161C=	XP_016871867.1:n.*161C=
NM_018344.6:c.*161C= MANE Select	NP_060814.4:n.*161C=
NM_001174098.2:c.*818C=	NP_001167569.1:n.*818C=
NM_001363518.2:c.*161C=	NP_001350447.1:n.*161C=
NR_033413.2:n.1557C=
NR_033414.2:n.1330C=