Canonical Allele Identifier: CA377114736

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121850A>G (hg19) ; chr10:g.71362093A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362093A>G , CM000672.2:g.71362093A>G	GRCh38
NC_000010.10:g.73121850A>G , CM000672.1:g.73121850A>G	GRCh37
NC_000010.9:g.72791856A>G	NCBI36
NG_017066.1:g.47841A>G
NG_017066.2:g.47835A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2389A>G
ENST00000373189.6:c.913A>G MANE Select	ENSP00000362285.5:p.Thr305Ala
ENST00000479577.2:c.679A>G	ENSP00000493995.1:p.Thr227Ala
ENST00000642198.1:c.*485A>G	ENSP00000494827.1:n.*485A>G
ENST00000642772.1:c.*94+5850A>G	ENSP00000495041.1:n.*94+5850A>G
ENST00000643042.1:c.534A>G	ENSP00000496674.1:n.534A>G
ENST00000643619.1:c.*496A>G	ENSP00000494378.1:n.*496A>G
ENST00000643752.1:c.*239A>G	ENSP00000495000.1:n.*239A>G
ENST00000644088.1:c.*234A>G	ENSP00000494066.1:n.*234A>G
ENST00000644591.1:c.*239A>G	ENSP00000496664.1:n.*239A>G
ENST00000644895.1:c.*99+5850A>G	ENSP00000493872.1:n.*99+5850A>G
ENST00000645345.1:c.*485A>G	ENSP00000495859.1:n.*485A>G
ENST00000647524.1:c.*496A>G	ENSP00000495077.1:n.*496A>G
ENST00000373189.5:c.913A>G	ENSP00000362285.5:p.Thr305Ala
ENST00000469204.1:n.410A>G
NM_001174098.1:c.*142A>G	NP_001167569.1:n.*142A>G
NM_018344.5:c.913A>G	NP_060814.4:p.Thr305Ala
NR_033413.1:n.887A>G
NR_033414.1:n.660A>G
XM_006717910.2:c.679A>G	XP_006717973.1:p.Thr227Ala
NM_001363518.1:c.679A>G	NP_001350447.1:p.Thr227Ala
XM_017016377.2:c.475A>G	XP_016871866.1:p.Thr159Ala
XM_017016378.2:c.295A>G	XP_016871867.1:p.Thr99Ala
NM_018344.6:c.913A>G MANE Select	NP_060814.4:p.Thr305Ala
NM_001174098.2:c.*142A>G	NP_001167569.1:n.*142A>G
NM_001363518.2:c.679A>G	NP_001350447.1:p.Thr227Ala
NR_033413.2:n.881A>G
NR_033414.2:n.654A>G