Canonical Allele Identifier: CA470281458

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122056G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362299G>C , CM000672.2:g.71362299G>C	GRCh38
NC_000010.10:g.73122056G>C , CM000672.1:g.73122056G>C	GRCh37
NC_000010.9:g.72792062G>C	NCBI36
NG_017066.1:g.48047G>C
NG_017066.2:g.48041G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2595G>C
ENST00000373189.6:c.1119G>C MANE Select	ENSP00000362285.5:p.Gly373=
ENST00000479577.2:c.885G>C	ENSP00000493995.1:p.Gly295=
ENST00000642198.1:c.*691G>C	ENSP00000494827.1:n.*691G>C
ENST00000642772.1:c.*94+6056G>C	ENSP00000495041.1:n.*94+6056G>C
ENST00000643042.1:c.740G>C	ENSP00000496674.1:n.740G>C
ENST00000643619.1:c.*702G>C	ENSP00000494378.1:n.*702G>C
ENST00000643752.1:c.*445G>C	ENSP00000495000.1:n.*445G>C
ENST00000644088.1:c.*440G>C	ENSP00000494066.1:n.*440G>C
ENST00000644591.1:c.*445G>C	ENSP00000496664.1:n.*445G>C
ENST00000644895.1:c.*99+6056G>C	ENSP00000493872.1:n.*99+6056G>C
ENST00000645345.1:c.*691G>C	ENSP00000495859.1:n.*691G>C
ENST00000647524.1:c.*702G>C	ENSP00000495077.1:n.*702G>C
ENST00000373189.5:c.1119G>C	ENSP00000362285.5:p.Gly373=
ENST00000469204.1:n.616G>C
NM_001174098.1:c.*348G>C	NP_001167569.1:n.*348G>C
NM_018344.5:c.1119G>C	NP_060814.4:p.Gly373=
NR_033413.1:n.1093G>C
NR_033414.1:n.866G>C
XM_006717910.2:c.885G>C	XP_006717973.1:p.Gly295=
NM_001363518.1:c.885G>C	NP_001350447.1:p.Gly295=
XM_017016377.2:c.681G>C	XP_016871866.1:p.Gly227=
XM_017016378.2:c.501G>C	XP_016871867.1:p.Gly167=
NM_018344.6:c.1119G>C MANE Select	NP_060814.4:p.Gly373=
NM_001174098.2:c.*348G>C	NP_001167569.1:n.*348G>C
NM_001363518.2:c.885G>C	NP_001350447.1:p.Gly295=
NR_033413.2:n.1087G>C
NR_033414.2:n.860G>C