Canonical Allele Identifier: CA377117147

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122199T>G (hg19) ; chr10:g.71362442T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362442T>G , CM000672.2:g.71362442T>G	GRCh38
NC_000010.10:g.73122199T>G , CM000672.1:g.73122199T>G	GRCh37
NC_000010.9:g.72792205T>G	NCBI36
NG_017066.1:g.48190T>G
NG_017066.2:g.48184T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2738T>G
ENST00000373189.6:c.1262T>G MANE Select	ENSP00000362285.5:p.Leu421Arg
ENST00000479577.2:c.1028T>G	ENSP00000493995.1:p.Leu343Arg
ENST00000642198.1:c.*834T>G	ENSP00000494827.1:n.*834T>G
ENST00000642772.1:c.*94+6199T>G	ENSP00000495041.1:n.*94+6199T>G
ENST00000643042.1:c.883T>G	ENSP00000496674.1:n.883T>G
ENST00000643619.1:c.*845T>G	ENSP00000494378.1:n.*845T>G
ENST00000643752.1:c.*588T>G	ENSP00000495000.1:n.*588T>G
ENST00000644088.1:c.*583T>G	ENSP00000494066.1:n.*583T>G
ENST00000644591.1:c.*588T>G	ENSP00000496664.1:n.*588T>G
ENST00000644895.1:c.*99+6199T>G	ENSP00000493872.1:n.*99+6199T>G
ENST00000645345.1:c.*834T>G	ENSP00000495859.1:n.*834T>G
ENST00000647524.1:c.*845T>G	ENSP00000495077.1:n.*845T>G
ENST00000373189.5:c.1262T>G	ENSP00000362285.5:p.Leu421Arg
ENST00000469204.1:n.759T>G
NM_001174098.1:c.*491T>G	NP_001167569.1:n.*491T>G
NM_018344.5:c.1262T>G	NP_060814.4:p.Leu421Arg
NR_033413.1:n.1236T>G
NR_033414.1:n.1009T>G
XM_006717910.2:c.1028T>G	XP_006717973.1:p.Leu343Arg
NM_001363518.1:c.1028T>G	NP_001350447.1:p.Leu343Arg
XM_017016377.2:c.824T>G	XP_016871866.1:p.Leu275Arg
XM_017016378.2:c.644T>G	XP_016871867.1:p.Leu215Arg
NM_018344.6:c.1262T>G MANE Select	NP_060814.4:p.Leu421Arg
NM_001174098.2:c.*491T>G	NP_001167569.1:n.*491T>G
NM_001363518.2:c.1028T>G	NP_001350447.1:p.Leu343Arg
NR_033413.2:n.1230T>G
NR_033414.2:n.1003T>G