Canonical Allele Identifier: CA1918678356

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362119C= , CM000672.2:g.71362119C=	GRCh38
NC_000010.10:g.73121876C= , CM000672.1:g.73121876C=	GRCh37
NC_000010.9:g.72791882C=	NCBI36
NG_017066.1:g.47867C=
NG_017066.2:g.47861C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2415C=
ENST00000373189.6:c.939C= MANE Select	ENSP00000362285.5:p.Thr313=
ENST00000479577.2:c.705C=	ENSP00000493995.1:p.Thr235=
ENST00000642198.1:c.*511C=	ENSP00000494827.1:n.*511C=
ENST00000642772.1:c.*94+5876C=	ENSP00000495041.1:n.*94+5876C=
ENST00000643042.1:c.560C=	ENSP00000496674.1:n.560C=
ENST00000643619.1:c.*522C=	ENSP00000494378.1:n.*522C=
ENST00000643752.1:c.*265C=	ENSP00000495000.1:n.*265C=
ENST00000644088.1:c.*260C=	ENSP00000494066.1:n.*260C=
ENST00000644591.1:c.*265C=	ENSP00000496664.1:n.*265C=
ENST00000644895.1:c.*99+5876C=	ENSP00000493872.1:n.*99+5876C=
ENST00000645345.1:c.*511C=	ENSP00000495859.1:n.*511C=
ENST00000647524.1:c.*522C=	ENSP00000495077.1:n.*522C=
ENST00000373189.5:c.939C=	ENSP00000362285.5:p.Thr313=
ENST00000469204.1:n.436C=
NM_001174098.1:c.*168C=	NP_001167569.1:n.*168C=
NM_018344.5:c.939C=	NP_060814.4:p.Thr313=
NR_033413.1:n.913C=
NR_033414.1:n.686C=
XM_006717910.2:c.705C=	XP_006717973.1:p.Thr235=
NM_001363518.1:c.705C=	NP_001350447.1:p.Thr235=
XM_017016377.2:c.501C=	XP_016871866.1:p.Thr167=
XM_017016378.2:c.321C=	XP_016871867.1:p.Thr107=
NM_018344.6:c.939C= MANE Select	NP_060814.4:p.Thr313=
NM_001174098.2:c.*168C=	NP_001167569.1:n.*168C=
NM_001363518.2:c.705C=	NP_001350447.1:p.Thr235=
NR_033413.2:n.907C=
NR_033414.2:n.680C=