Canonical Allele Identifier: CA470280800

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121753T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361996T>C , CM000672.2:g.71361996T>C	GRCh38
NC_000010.10:g.73121753T>C , CM000672.1:g.73121753T>C	GRCh37
NC_000010.9:g.72791759T>C	NCBI36
NG_017066.1:g.47744T>C
NG_017066.2:g.47738T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2292T>C
ENST00000373189.6:c.816T>C MANE Select	ENSP00000362285.5:p.Gly272=
ENST00000479577.2:c.582T>C	ENSP00000493995.1:p.Gly194=
ENST00000642198.1:c.*388T>C	ENSP00000494827.1:n.*388T>C
ENST00000642772.1:c.*94+5753T>C	ENSP00000495041.1:n.*94+5753T>C
ENST00000643042.1:c.437T>C	ENSP00000496674.1:n.437T>C
ENST00000643619.1:c.*399T>C	ENSP00000494378.1:n.*399T>C
ENST00000643752.1:c.*142T>C	ENSP00000495000.1:n.*142T>C
ENST00000644088.1:c.*137T>C	ENSP00000494066.1:n.*137T>C
ENST00000644591.1:c.*142T>C	ENSP00000496664.1:n.*142T>C
ENST00000644895.1:c.*99+5753T>C	ENSP00000493872.1:n.*99+5753T>C
ENST00000645345.1:c.*388T>C	ENSP00000495859.1:n.*388T>C
ENST00000647524.1:c.*399T>C	ENSP00000495077.1:n.*399T>C
ENST00000373189.5:c.816T>C	ENSP00000362285.5:p.Gly272=
ENST00000469204.1:n.313T>C
NM_001174098.1:c.*45T>C	NP_001167569.1:n.*45T>C
NM_018344.5:c.816T>C	NP_060814.4:p.Gly272=
NR_033413.1:n.790T>C
NR_033414.1:n.563T>C
XM_006717910.2:c.582T>C	XP_006717973.1:p.Gly194=
NM_001363518.1:c.582T>C	NP_001350447.1:p.Gly194=
XM_017016377.2:c.378T>C	XP_016871866.1:p.Gly126=
XM_017016378.2:c.198T>C	XP_016871867.1:p.Gly66=
NM_018344.6:c.816T>C MANE Select	NP_060814.4:p.Gly272=
NM_001174098.2:c.*45T>C	NP_001167569.1:n.*45T>C
NM_001363518.2:c.582T>C	NP_001350447.1:p.Gly194=
NR_033413.2:n.784T>C
NR_033414.2:n.557T>C