Canonical Allele Identifier: CA1918678280

Gene: SLC29A3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361964A= , CM000672.2:g.71361964A=	GRCh38
NC_000010.10:g.73121721A= , CM000672.1:g.73121721A=	GRCh37
NC_000010.9:g.72791727A=	NCBI36
NG_017066.1:g.47712A=
NG_017066.2:g.47706A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2260A=
ENST00000373189.6:c.784A= MANE Select	ENSP00000362285.5:p.Arg262=
ENST00000479577.2:c.550A=	ENSP00000493995.1:p.Arg184=
ENST00000642198.1:c.*356A=	ENSP00000494827.1:n.*356A=
ENST00000642772.1:c.*94+5721A=	ENSP00000495041.1:n.*94+5721A=
ENST00000643042.1:c.405A=	ENSP00000496674.1:n.405A=
ENST00000643619.1:c.*367A=	ENSP00000494378.1:n.*367A=
ENST00000643752.1:c.*110A=	ENSP00000495000.1:n.*110A=
ENST00000644088.1:c.*105A=	ENSP00000494066.1:n.*105A=
ENST00000644591.1:c.*110A=	ENSP00000496664.1:n.*110A=
ENST00000644895.1:c.*99+5721A=	ENSP00000493872.1:n.*99+5721A=
ENST00000645345.1:c.*356A=	ENSP00000495859.1:n.*356A=
ENST00000647524.1:c.*367A=	ENSP00000495077.1:n.*367A=
ENST00000373189.5:c.784A=	ENSP00000362285.5:p.Arg262=
ENST00000469204.1:n.281A=
NM_001174098.1:c.*13A=	NP_001167569.1:n.*13A=
NM_018344.5:c.784A=	NP_060814.4:p.Arg262=
NR_033413.1:n.758A=
NR_033414.1:n.531A=
XM_006717910.2:c.550A=	XP_006717973.1:p.Arg184=
NM_001363518.1:c.550A=	NP_001350447.1:p.Arg184=
XM_017016377.2:c.346A=	XP_016871866.1:p.Arg116=
XM_017016378.2:c.166A=	XP_016871867.1:p.Arg56=
NM_018344.6:c.784A= MANE Select	NP_060814.4:p.Arg262=
NM_001174098.2:c.*13A=	NP_001167569.1:n.*13A=
NM_001363518.2:c.550A=	NP_001350447.1:p.Arg184=
NR_033413.2:n.752A=
NR_033414.2:n.525A=