Canonical Allele Identifier: CA377114302

Gene: SLC29A3

Linked Data

• gnomAD v4: 10-71362045-A-G
• MyVariant Identifiers: chr10:g.73121802A>G (hg19) ; chr10:g.71362045A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362045A>G , CM000672.2:g.71362045A>G	GRCh38
NC_000010.10:g.73121802A>G , CM000672.1:g.73121802A>G	GRCh37
NC_000010.9:g.72791808A>G	NCBI36
NG_017066.1:g.47793A>G
NG_017066.2:g.47787A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2341A>G
ENST00000373189.6:c.865A>G MANE Select	ENSP00000362285.5:p.Arg289Gly
ENST00000479577.2:c.631A>G	ENSP00000493995.1:p.Arg211Gly
ENST00000642198.1:c.*437A>G	ENSP00000494827.1:n.*437A>G
ENST00000642772.1:c.*94+5802A>G	ENSP00000495041.1:n.*94+5802A>G
ENST00000643042.1:c.486A>G	ENSP00000496674.1:n.486A>G
ENST00000643619.1:c.*448A>G	ENSP00000494378.1:n.*448A>G
ENST00000643752.1:c.*191A>G	ENSP00000495000.1:n.*191A>G
ENST00000644088.1:c.*186A>G	ENSP00000494066.1:n.*186A>G
ENST00000644591.1:c.*191A>G	ENSP00000496664.1:n.*191A>G
ENST00000644895.1:c.*99+5802A>G	ENSP00000493872.1:n.*99+5802A>G
ENST00000645345.1:c.*437A>G	ENSP00000495859.1:n.*437A>G
ENST00000647524.1:c.*448A>G	ENSP00000495077.1:n.*448A>G
ENST00000373189.5:c.865A>G	ENSP00000362285.5:p.Arg289Gly
ENST00000469204.1:n.362A>G
NM_001174098.1:c.*94A>G	NP_001167569.1:n.*94A>G
NM_018344.5:c.865A>G	NP_060814.4:p.Arg289Gly
NR_033413.1:n.839A>G
NR_033414.1:n.612A>G
XM_006717910.2:c.631A>G	XP_006717973.1:p.Arg211Gly
NM_001363518.1:c.631A>G	NP_001350447.1:p.Arg211Gly
XM_017016377.2:c.427A>G	XP_016871866.1:p.Arg143Gly
XM_017016378.2:c.247A>G	XP_016871867.1:p.Arg83Gly
NM_018344.6:c.865A>G MANE Select	NP_060814.4:p.Arg289Gly
NM_001174098.2:c.*94A>G	NP_001167569.1:n.*94A>G
NM_001363518.2:c.631A>G	NP_001350447.1:p.Arg211Gly
NR_033413.2:n.833A>G
NR_033414.2:n.606A>G