Canonical Allele Identifier: CA377114962

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121871G>A (hg19) ; chr10:g.71362114G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362114G>A , CM000672.2:g.71362114G>A	GRCh38
NC_000010.10:g.73121871G>A , CM000672.1:g.73121871G>A	GRCh37
NC_000010.9:g.72791877G>A	NCBI36
NG_017066.1:g.47862G>A
NG_017066.2:g.47856G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2410G>A
ENST00000373189.6:c.934G>A MANE Select	ENSP00000362285.5:p.Val312Ile
ENST00000479577.2:c.700G>A	ENSP00000493995.1:p.Val234Ile
ENST00000642198.1:c.*506G>A	ENSP00000494827.1:n.*506G>A
ENST00000642772.1:c.*94+5871G>A	ENSP00000495041.1:n.*94+5871G>A
ENST00000643042.1:c.555G>A	ENSP00000496674.1:n.555G>A
ENST00000643619.1:c.*517G>A	ENSP00000494378.1:n.*517G>A
ENST00000643752.1:c.*260G>A	ENSP00000495000.1:n.*260G>A
ENST00000644088.1:c.*255G>A	ENSP00000494066.1:n.*255G>A
ENST00000644591.1:c.*260G>A	ENSP00000496664.1:n.*260G>A
ENST00000644895.1:c.*99+5871G>A	ENSP00000493872.1:n.*99+5871G>A
ENST00000645345.1:c.*506G>A	ENSP00000495859.1:n.*506G>A
ENST00000647524.1:c.*517G>A	ENSP00000495077.1:n.*517G>A
ENST00000373189.5:c.934G>A	ENSP00000362285.5:p.Val312Ile
ENST00000469204.1:n.431G>A
NM_001174098.1:c.*163G>A	NP_001167569.1:n.*163G>A
NM_018344.5:c.934G>A	NP_060814.4:p.Val312Ile
NR_033413.1:n.908G>A
NR_033414.1:n.681G>A
XM_006717910.2:c.700G>A	XP_006717973.1:p.Val234Ile
NM_001363518.1:c.700G>A	NP_001350447.1:p.Val234Ile
XM_017016377.2:c.496G>A	XP_016871866.1:p.Val166Ile
XM_017016378.2:c.316G>A	XP_016871867.1:p.Val106Ile
NM_018344.6:c.934G>A MANE Select	NP_060814.4:p.Val312Ile
NM_001174098.2:c.*163G>A	NP_001167569.1:n.*163G>A
NM_001363518.2:c.700G>A	NP_001350447.1:p.Val234Ile
NR_033413.2:n.902G>A
NR_033414.2:n.675G>A