Canonical Allele Identifier: CA1918678283

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361969T= , CM000672.2:g.71361969T=	GRCh38
NC_000010.10:g.73121726T= , CM000672.1:g.73121726T=	GRCh37
NC_000010.9:g.72791732T=	NCBI36
NG_017066.1:g.47717T=
NG_017066.2:g.47711T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2265T=
ENST00000373189.6:c.789T= MANE Select	ENSP00000362285.5:p.Pro263=
ENST00000479577.2:c.555T=	ENSP00000493995.1:p.Pro185=
ENST00000642198.1:c.*361T=	ENSP00000494827.1:n.*361T=
ENST00000642772.1:c.*94+5726T=	ENSP00000495041.1:n.*94+5726T=
ENST00000643042.1:c.410T=	ENSP00000496674.1:n.410T=
ENST00000643619.1:c.*372T=	ENSP00000494378.1:n.*372T=
ENST00000643752.1:c.*115T=	ENSP00000495000.1:n.*115T=
ENST00000644088.1:c.*110T=	ENSP00000494066.1:n.*110T=
ENST00000644591.1:c.*115T=	ENSP00000496664.1:n.*115T=
ENST00000644895.1:c.*99+5726T=	ENSP00000493872.1:n.*99+5726T=
ENST00000645345.1:c.*361T=	ENSP00000495859.1:n.*361T=
ENST00000647524.1:c.*372T=	ENSP00000495077.1:n.*372T=
ENST00000373189.5:c.789T=	ENSP00000362285.5:p.Pro263=
ENST00000469204.1:n.286T=
NM_001174098.1:c.*18T=	NP_001167569.1:n.*18T=
NM_018344.5:c.789T=	NP_060814.4:p.Pro263=
NR_033413.1:n.763T=
NR_033414.1:n.536T=
XM_006717910.2:c.555T=	XP_006717973.1:p.Pro185=
NM_001363518.1:c.555T=	NP_001350447.1:p.Pro185=
XM_017016377.2:c.351T=	XP_016871866.1:p.Pro117=
XM_017016378.2:c.171T=	XP_016871867.1:p.Pro57=
NM_018344.6:c.789T= MANE Select	NP_060814.4:p.Pro263=
NM_001174098.2:c.*18T=	NP_001167569.1:n.*18T=
NM_001363518.2:c.555T=	NP_001350447.1:p.Pro185=
NR_033413.2:n.757T=
NR_033414.2:n.530T=