Canonical Allele Identifier: CA470280728

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121721A>C (hg19)

Genomic Alleles

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

Transcript Alleles

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