Canonical Allele Identifier: CA377117172

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122213A>G (hg19) ; chr10:g.71362456A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362456A>G , CM000672.2:g.71362456A>G	GRCh38
NC_000010.10:g.73122213A>G , CM000672.1:g.73122213A>G	GRCh37
NC_000010.9:g.72792219A>G	NCBI36
NG_017066.1:g.48204A>G
NG_017066.2:g.48198A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2752A>G
ENST00000373189.6:c.1276A>G MANE Select	ENSP00000362285.5:p.Asn426Asp
ENST00000479577.2:c.1042A>G	ENSP00000493995.1:p.Asn348Asp
ENST00000642198.1:c.*848A>G	ENSP00000494827.1:n.*848A>G
ENST00000642772.1:c.*94+6213A>G	ENSP00000495041.1:n.*94+6213A>G
ENST00000643042.1:c.897A>G	ENSP00000496674.1:n.897A>G
ENST00000643619.1:c.*859A>G	ENSP00000494378.1:n.*859A>G
ENST00000643752.1:c.*602A>G	ENSP00000495000.1:n.*602A>G
ENST00000644088.1:c.*597A>G	ENSP00000494066.1:n.*597A>G
ENST00000644591.1:c.*602A>G	ENSP00000496664.1:n.*602A>G
ENST00000644895.1:c.*99+6213A>G	ENSP00000493872.1:n.*99+6213A>G
ENST00000645345.1:c.*848A>G	ENSP00000495859.1:n.*848A>G
ENST00000647524.1:c.*859A>G	ENSP00000495077.1:n.*859A>G
ENST00000373189.5:c.1276A>G	ENSP00000362285.5:p.Asn426Asp
ENST00000469204.1:n.773A>G
NM_001174098.1:c.*505A>G	NP_001167569.1:n.*505A>G
NM_018344.5:c.1276A>G	NP_060814.4:p.Asn426Asp
NR_033413.1:n.1250A>G
NR_033414.1:n.1023A>G
XM_006717910.2:c.1042A>G	XP_006717973.1:p.Asn348Asp
NM_001363518.1:c.1042A>G	NP_001350447.1:p.Asn348Asp
XM_017016377.2:c.838A>G	XP_016871866.1:p.Asn280Asp
XM_017016378.2:c.658A>G	XP_016871867.1:p.Asn220Asp
NM_018344.6:c.1276A>G MANE Select	NP_060814.4:p.Asn426Asp
NM_001174098.2:c.*505A>G	NP_001167569.1:n.*505A>G
NM_001363518.2:c.1042A>G	NP_001350447.1:p.Asn348Asp
NR_033413.2:n.1244A>G
NR_033414.2:n.1017A>G