Canonical Allele Identifier: CA377115441

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121935T>G (hg19) ; chr10:g.71362178T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362178T>G , CM000672.2:g.71362178T>G	GRCh38
NC_000010.10:g.73121935T>G , CM000672.1:g.73121935T>G	GRCh37
NC_000010.9:g.72791941T>G	NCBI36
NG_017066.1:g.47926T>G
NG_017066.2:g.47920T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2474T>G
ENST00000373189.6:c.998T>G MANE Select	ENSP00000362285.5:p.Leu333Arg
ENST00000479577.2:c.764T>G	ENSP00000493995.1:p.Leu255Arg
ENST00000642198.1:c.*570T>G	ENSP00000494827.1:n.*570T>G
ENST00000642772.1:c.*94+5935T>G	ENSP00000495041.1:n.*94+5935T>G
ENST00000643042.1:c.619T>G	ENSP00000496674.1:n.619T>G
ENST00000643619.1:c.*581T>G	ENSP00000494378.1:n.*581T>G
ENST00000643752.1:c.*324T>G	ENSP00000495000.1:n.*324T>G
ENST00000644088.1:c.*319T>G	ENSP00000494066.1:n.*319T>G
ENST00000644591.1:c.*324T>G	ENSP00000496664.1:n.*324T>G
ENST00000644895.1:c.*99+5935T>G	ENSP00000493872.1:n.*99+5935T>G
ENST00000645345.1:c.*570T>G	ENSP00000495859.1:n.*570T>G
ENST00000647524.1:c.*581T>G	ENSP00000495077.1:n.*581T>G
ENST00000373189.5:c.998T>G	ENSP00000362285.5:p.Leu333Arg
ENST00000469204.1:n.495T>G
NM_001174098.1:c.*227T>G	NP_001167569.1:n.*227T>G
NM_018344.5:c.998T>G	NP_060814.4:p.Leu333Arg
NR_033413.1:n.972T>G
NR_033414.1:n.745T>G
XM_006717910.2:c.764T>G	XP_006717973.1:p.Leu255Arg
NM_001363518.1:c.764T>G	NP_001350447.1:p.Leu255Arg
XM_017016377.2:c.560T>G	XP_016871866.1:p.Leu187Arg
XM_017016378.2:c.380T>G	XP_016871867.1:p.Leu127Arg
NM_018344.6:c.998T>G MANE Select	NP_060814.4:p.Leu333Arg
NM_001174098.2:c.*227T>G	NP_001167569.1:n.*227T>G
NM_001363518.2:c.764T>G	NP_001350447.1:p.Leu255Arg
NR_033413.2:n.966T>G
NR_033414.2:n.739T>G