Canonical Allele Identifier: CA377113938

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121751G>C (hg19) ; chr10:g.71361994G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71361994G>C , CM000672.2:g.71361994G>C	GRCh38
NC_000010.10:g.73121751G>C , CM000672.1:g.73121751G>C	GRCh37
NC_000010.9:g.72791757G>C	NCBI36
NG_017066.1:g.47742G>C
NG_017066.2:g.47736G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2290G>C
ENST00000373189.6:c.814G>C MANE Select	ENSP00000362285.5:p.Gly272Arg
ENST00000479577.2:c.580G>C	ENSP00000493995.1:p.Gly194Arg
ENST00000642198.1:c.*386G>C	ENSP00000494827.1:n.*386G>C
ENST00000642772.1:c.*94+5751G>C	ENSP00000495041.1:n.*94+5751G>C
ENST00000643042.1:c.435G>C	ENSP00000496674.1:n.435G>C
ENST00000643619.1:c.*397G>C	ENSP00000494378.1:n.*397G>C
ENST00000643752.1:c.*140G>C	ENSP00000495000.1:n.*140G>C
ENST00000644088.1:c.*135G>C	ENSP00000494066.1:n.*135G>C
ENST00000644591.1:c.*140G>C	ENSP00000496664.1:n.*140G>C
ENST00000644895.1:c.*99+5751G>C	ENSP00000493872.1:n.*99+5751G>C
ENST00000645345.1:c.*386G>C	ENSP00000495859.1:n.*386G>C
ENST00000647524.1:c.*397G>C	ENSP00000495077.1:n.*397G>C
ENST00000373189.5:c.814G>C	ENSP00000362285.5:p.Gly272Arg
ENST00000469204.1:n.311G>C
NM_001174098.1:c.*43G>C	NP_001167569.1:n.*43G>C
NM_018344.5:c.814G>C	NP_060814.4:p.Gly272Arg
NR_033413.1:n.788G>C
NR_033414.1:n.561G>C
XM_006717910.2:c.580G>C	XP_006717973.1:p.Gly194Arg
NM_001363518.1:c.580G>C	NP_001350447.1:p.Gly194Arg
XM_017016377.2:c.376G>C	XP_016871866.1:p.Gly126Arg
XM_017016378.2:c.196G>C	XP_016871867.1:p.Gly66Arg
NM_018344.6:c.814G>C MANE Select	NP_060814.4:p.Gly272Arg
NM_001174098.2:c.*43G>C	NP_001167569.1:n.*43G>C
NM_001363518.2:c.580G>C	NP_001350447.1:p.Gly194Arg
NR_033413.2:n.782G>C
NR_033414.2:n.555G>C