Canonical Allele Identifier: CA377114055

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121767C>G (hg19) ; chr10:g.71362010C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362010C>G , CM000672.2:g.71362010C>G	GRCh38
NC_000010.10:g.73121767C>G , CM000672.1:g.73121767C>G	GRCh37
NC_000010.9:g.72791773C>G	NCBI36
NG_017066.1:g.47758C>G
NG_017066.2:g.47752C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2306C>G
ENST00000373189.6:c.830C>G MANE Select	ENSP00000362285.5:p.Pro277Arg
ENST00000479577.2:c.596C>G	ENSP00000493995.1:p.Pro199Arg
ENST00000642198.1:c.*402C>G	ENSP00000494827.1:n.*402C>G
ENST00000642772.1:c.*94+5767C>G	ENSP00000495041.1:n.*94+5767C>G
ENST00000643042.1:c.451C>G	ENSP00000496674.1:n.451C>G
ENST00000643619.1:c.*413C>G	ENSP00000494378.1:n.*413C>G
ENST00000643752.1:c.*156C>G	ENSP00000495000.1:n.*156C>G
ENST00000644088.1:c.*151C>G	ENSP00000494066.1:n.*151C>G
ENST00000644591.1:c.*156C>G	ENSP00000496664.1:n.*156C>G
ENST00000644895.1:c.*99+5767C>G	ENSP00000493872.1:n.*99+5767C>G
ENST00000645345.1:c.*402C>G	ENSP00000495859.1:n.*402C>G
ENST00000647524.1:c.*413C>G	ENSP00000495077.1:n.*413C>G
ENST00000373189.5:c.830C>G	ENSP00000362285.5:p.Pro277Arg
ENST00000469204.1:n.327C>G
NM_001174098.1:c.*59C>G	NP_001167569.1:n.*59C>G
NM_018344.5:c.830C>G	NP_060814.4:p.Pro277Arg
NR_033413.1:n.804C>G
NR_033414.1:n.577C>G
XM_006717910.2:c.596C>G	XP_006717973.1:p.Pro199Arg
NM_001363518.1:c.596C>G	NP_001350447.1:p.Pro199Arg
XM_017016377.2:c.392C>G	XP_016871866.1:p.Pro131Arg
XM_017016378.2:c.212C>G	XP_016871867.1:p.Pro71Arg
NM_018344.6:c.830C>G MANE Select	NP_060814.4:p.Pro277Arg
NM_001174098.2:c.*59C>G	NP_001167569.1:n.*59C>G
NM_001363518.2:c.596C>G	NP_001350447.1:p.Pro199Arg
NR_033413.2:n.798C>G
NR_033414.2:n.571C>G