Canonical Allele Identifier: CA1918678462

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362349T= , CM000672.2:g.71362349T=	GRCh38
NC_000010.10:g.73122106T= , CM000672.1:g.73122106T=	GRCh37
NC_000010.9:g.72792112T=	NCBI36
NG_017066.1:g.48097T=
NG_017066.2:g.48091T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2645T=
ENST00000373189.6:c.1169T= MANE Select	ENSP00000362285.5:p.Ile390=
ENST00000479577.2:c.935T=	ENSP00000493995.1:p.Ile312=
ENST00000642198.1:c.*741T=	ENSP00000494827.1:n.*741T=
ENST00000642772.1:c.*94+6106T=	ENSP00000495041.1:n.*94+6106T=
ENST00000643042.1:c.790T=	ENSP00000496674.1:n.790T=
ENST00000643619.1:c.*752T=	ENSP00000494378.1:n.*752T=
ENST00000643752.1:c.*495T=	ENSP00000495000.1:n.*495T=
ENST00000644088.1:c.*490T=	ENSP00000494066.1:n.*490T=
ENST00000644591.1:c.*495T=	ENSP00000496664.1:n.*495T=
ENST00000644895.1:c.*99+6106T=	ENSP00000493872.1:n.*99+6106T=
ENST00000645345.1:c.*741T=	ENSP00000495859.1:n.*741T=
ENST00000647524.1:c.*752T=	ENSP00000495077.1:n.*752T=
ENST00000373189.5:c.1169T=	ENSP00000362285.5:p.Ile390=
ENST00000469204.1:n.666T=
NM_001174098.1:c.*398T=	NP_001167569.1:n.*398T=
NM_018344.5:c.1169T=	NP_060814.4:p.Ile390=
NR_033413.1:n.1143T=
NR_033414.1:n.916T=
XM_006717910.2:c.935T=	XP_006717973.1:p.Ile312=
NM_001363518.1:c.935T=	NP_001350447.1:p.Ile312=
XM_017016377.2:c.731T=	XP_016871866.1:p.Ile244=
XM_017016378.2:c.551T=	XP_016871867.1:p.Ile184=
NM_018344.6:c.1169T= MANE Select	NP_060814.4:p.Ile390=
NM_001174098.2:c.*398T=	NP_001167569.1:n.*398T=
NM_001363518.2:c.935T=	NP_001350447.1:p.Ile312=
NR_033413.2:n.1137T=
NR_033414.2:n.910T=