Canonical Allele Identifier: CA1918678352

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362111T= , CM000672.2:g.71362111T=	GRCh38
NC_000010.10:g.73121868T= , CM000672.1:g.73121868T=	GRCh37
NC_000010.9:g.72791874T=	NCBI36
NG_017066.1:g.47859T=
NG_017066.2:g.47853T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2407T=
ENST00000373189.6:c.931T= MANE Select	ENSP00000362285.5:p.Cys311=
ENST00000479577.2:c.697T=	ENSP00000493995.1:p.Cys233=
ENST00000642198.1:c.*503T=	ENSP00000494827.1:n.*503T=
ENST00000642772.1:c.*94+5868T=	ENSP00000495041.1:n.*94+5868T=
ENST00000643042.1:c.552T=	ENSP00000496674.1:n.552T=
ENST00000643619.1:c.*514T=	ENSP00000494378.1:n.*514T=
ENST00000643752.1:c.*257T=	ENSP00000495000.1:n.*257T=
ENST00000644088.1:c.*252T=	ENSP00000494066.1:n.*252T=
ENST00000644591.1:c.*257T=	ENSP00000496664.1:n.*257T=
ENST00000644895.1:c.*99+5868T=	ENSP00000493872.1:n.*99+5868T=
ENST00000645345.1:c.*503T=	ENSP00000495859.1:n.*503T=
ENST00000647524.1:c.*514T=	ENSP00000495077.1:n.*514T=
ENST00000373189.5:c.931T=	ENSP00000362285.5:p.Cys311=
ENST00000469204.1:n.428T=
NM_001174098.1:c.*160T=	NP_001167569.1:n.*160T=
NM_018344.5:c.931T=	NP_060814.4:p.Cys311=
NR_033413.1:n.905T=
NR_033414.1:n.678T=
XM_006717910.2:c.697T=	XP_006717973.1:p.Cys233=
NM_001363518.1:c.697T=	NP_001350447.1:p.Cys233=
XM_017016377.2:c.493T=	XP_016871866.1:p.Cys165=
XM_017016378.2:c.313T=	XP_016871867.1:p.Cys105=
NM_018344.6:c.931T= MANE Select	NP_060814.4:p.Cys311=
NM_001174098.2:c.*160T=	NP_001167569.1:n.*160T=
NM_001363518.2:c.697T=	NP_001350447.1:p.Cys233=
NR_033413.2:n.899T=
NR_033414.2:n.672T=