Canonical Allele Identifier: CA1918678339

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362082T= , CM000672.2:g.71362082T=	GRCh38
NC_000010.10:g.73121839T= , CM000672.1:g.73121839T=	GRCh37
NC_000010.9:g.72791845T=	NCBI36
NG_017066.1:g.47830T=
NG_017066.2:g.47824T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2378T=
ENST00000373189.6:c.902T= MANE Select	ENSP00000362285.5:p.Ile301=
ENST00000479577.2:c.668T=	ENSP00000493995.1:p.Ile223=
ENST00000642198.1:c.*474T=	ENSP00000494827.1:n.*474T=
ENST00000642772.1:c.*94+5839T=	ENSP00000495041.1:n.*94+5839T=
ENST00000643042.1:c.523T=	ENSP00000496674.1:n.523T=
ENST00000643619.1:c.*485T=	ENSP00000494378.1:n.*485T=
ENST00000643752.1:c.*228T=	ENSP00000495000.1:n.*228T=
ENST00000644088.1:c.*223T=	ENSP00000494066.1:n.*223T=
ENST00000644591.1:c.*228T=	ENSP00000496664.1:n.*228T=
ENST00000644895.1:c.*99+5839T=	ENSP00000493872.1:n.*99+5839T=
ENST00000645345.1:c.*474T=	ENSP00000495859.1:n.*474T=
ENST00000647524.1:c.*485T=	ENSP00000495077.1:n.*485T=
ENST00000373189.5:c.902T=	ENSP00000362285.5:p.Ile301=
ENST00000469204.1:n.399T=
NM_001174098.1:c.*131T=	NP_001167569.1:n.*131T=
NM_018344.5:c.902T=	NP_060814.4:p.Ile301=
NR_033413.1:n.876T=
NR_033414.1:n.649T=
XM_006717910.2:c.668T=	XP_006717973.1:p.Ile223=
NM_001363518.1:c.668T=	NP_001350447.1:p.Ile223=
XM_017016377.2:c.464T=	XP_016871866.1:p.Ile155=
XM_017016378.2:c.284T=	XP_016871867.1:p.Ile95=
NM_018344.6:c.902T= MANE Select	NP_060814.4:p.Ile301=
NM_001174098.2:c.*131T=	NP_001167569.1:n.*131T=
NM_001363518.2:c.668T=	NP_001350447.1:p.Ile223=
NR_033413.2:n.870T=
NR_033414.2:n.643T=