Canonical Allele Identifier: CA377115230

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121908C>G (hg19) ; chr10:g.71362151C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362151C>G , CM000672.2:g.71362151C>G	GRCh38
NC_000010.10:g.73121908C>G , CM000672.1:g.73121908C>G	GRCh37
NC_000010.9:g.72791914C>G	NCBI36
NG_017066.1:g.47899C>G
NG_017066.2:g.47893C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2447C>G
ENST00000373189.6:c.971C>G MANE Select	ENSP00000362285.5:p.Pro324Arg
ENST00000479577.2:c.737C>G	ENSP00000493995.1:p.Pro246Arg
ENST00000642198.1:c.*543C>G	ENSP00000494827.1:n.*543C>G
ENST00000642772.1:c.*94+5908C>G	ENSP00000495041.1:n.*94+5908C>G
ENST00000643042.1:c.592C>G	ENSP00000496674.1:n.592C>G
ENST00000643619.1:c.*554C>G	ENSP00000494378.1:n.*554C>G
ENST00000643752.1:c.*297C>G	ENSP00000495000.1:n.*297C>G
ENST00000644088.1:c.*292C>G	ENSP00000494066.1:n.*292C>G
ENST00000644591.1:c.*297C>G	ENSP00000496664.1:n.*297C>G
ENST00000644895.1:c.*99+5908C>G	ENSP00000493872.1:n.*99+5908C>G
ENST00000645345.1:c.*543C>G	ENSP00000495859.1:n.*543C>G
ENST00000647524.1:c.*554C>G	ENSP00000495077.1:n.*554C>G
ENST00000373189.5:c.971C>G	ENSP00000362285.5:p.Pro324Arg
ENST00000469204.1:n.468C>G
NM_001174098.1:c.*200C>G	NP_001167569.1:n.*200C>G
NM_018344.5:c.971C>G	NP_060814.4:p.Pro324Arg
NR_033413.1:n.945C>G
NR_033414.1:n.718C>G
XM_006717910.2:c.737C>G	XP_006717973.1:p.Pro246Arg
NM_001363518.1:c.737C>G	NP_001350447.1:p.Pro246Arg
XM_017016377.2:c.533C>G	XP_016871866.1:p.Pro178Arg
XM_017016378.2:c.353C>G	XP_016871867.1:p.Pro118Arg
NM_018344.6:c.971C>G MANE Select	NP_060814.4:p.Pro324Arg
NM_001174098.2:c.*200C>G	NP_001167569.1:n.*200C>G
NM_001363518.2:c.737C>G	NP_001350447.1:p.Pro246Arg
NR_033413.2:n.939C>G
NR_033414.2:n.712C>G