Canonical Allele Identifier: CA377117206

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122231C>G (hg19) ; chr10:g.71362474C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362474C>G , CM000672.2:g.71362474C>G	GRCh38
NC_000010.10:g.73122231C>G , CM000672.1:g.73122231C>G	GRCh37
NC_000010.9:g.72792237C>G	NCBI36
NG_017066.1:g.48222C>G
NG_017066.2:g.48216C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2770C>G
ENST00000373189.6:c.1294C>G MANE Select	ENSP00000362285.5:p.Leu432Val
ENST00000479577.2:c.1060C>G	ENSP00000493995.1:p.Leu354Val
ENST00000642198.1:c.*866C>G	ENSP00000494827.1:n.*866C>G
ENST00000642772.1:c.*94+6231C>G	ENSP00000495041.1:n.*94+6231C>G
ENST00000643042.1:c.915C>G	ENSP00000496674.1:n.915C>G
ENST00000643619.1:c.*877C>G	ENSP00000494378.1:n.*877C>G
ENST00000643752.1:c.*620C>G	ENSP00000495000.1:n.*620C>G
ENST00000644088.1:c.*615C>G	ENSP00000494066.1:n.*615C>G
ENST00000644591.1:c.*620C>G	ENSP00000496664.1:n.*620C>G
ENST00000644895.1:c.*99+6231C>G	ENSP00000493872.1:n.*99+6231C>G
ENST00000645345.1:c.*866C>G	ENSP00000495859.1:n.*866C>G
ENST00000647524.1:c.*877C>G	ENSP00000495077.1:n.*877C>G
ENST00000373189.5:c.1294C>G	ENSP00000362285.5:p.Leu432Val
ENST00000469204.1:n.791C>G
NM_001174098.1:c.*523C>G	NP_001167569.1:n.*523C>G
NM_018344.5:c.1294C>G	NP_060814.4:p.Leu432Val
NR_033413.1:n.1268C>G
NR_033414.1:n.1041C>G
XM_006717910.2:c.1060C>G	XP_006717973.1:p.Leu354Val
NM_001363518.1:c.1060C>G	NP_001350447.1:p.Leu354Val
XM_017016377.2:c.856C>G	XP_016871866.1:p.Leu286Val
XM_017016378.2:c.676C>G	XP_016871867.1:p.Leu226Val
NM_018344.6:c.1294C>G MANE Select	NP_060814.4:p.Leu432Val
NM_001174098.2:c.*523C>G	NP_001167569.1:n.*523C>G
NM_001363518.2:c.1060C>G	NP_001350447.1:p.Leu354Val
NR_033413.2:n.1262C>G
NR_033414.2:n.1035C>G