Canonical Allele Identifier: CA377116677

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122049T>A (hg19) ; chr10:g.71362292T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362292T>A , CM000672.2:g.71362292T>A	GRCh38
NC_000010.10:g.73122049T>A , CM000672.1:g.73122049T>A	GRCh37
NC_000010.9:g.72792055T>A	NCBI36
NG_017066.1:g.48040T>A
NG_017066.2:g.48034T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000697843.1:n.2588T>A
ENST00000373189.6:c.1112T>A MANE Select	ENSP00000362285.5:p.Val371Glu
ENST00000479577.2:c.878T>A	ENSP00000493995.1:p.Val293Glu
ENST00000642198.1:c.*684T>A	ENSP00000494827.1:n.*684T>A
ENST00000642772.1:c.*94+6049T>A	ENSP00000495041.1:n.*94+6049T>A
ENST00000643042.1:c.733T>A	ENSP00000496674.1:n.733T>A
ENST00000643619.1:c.*695T>A	ENSP00000494378.1:n.*695T>A
ENST00000643752.1:c.*438T>A	ENSP00000495000.1:n.*438T>A
ENST00000644088.1:c.*433T>A	ENSP00000494066.1:n.*433T>A
ENST00000644591.1:c.*438T>A	ENSP00000496664.1:n.*438T>A
ENST00000644895.1:c.*99+6049T>A	ENSP00000493872.1:n.*99+6049T>A
ENST00000645345.1:c.*684T>A	ENSP00000495859.1:n.*684T>A
ENST00000647524.1:c.*695T>A	ENSP00000495077.1:n.*695T>A
ENST00000373189.5:c.1112T>A	ENSP00000362285.5:p.Val371Glu
ENST00000469204.1:n.609T>A
NM_001174098.1:c.*341T>A	NP_001167569.1:n.*341T>A
NM_018344.5:c.1112T>A	NP_060814.4:p.Val371Glu
NR_033413.1:n.1086T>A
NR_033414.1:n.859T>A
XM_006717910.2:c.878T>A	XP_006717973.1:p.Val293Glu
NM_001363518.1:c.878T>A	NP_001350447.1:p.Val293Glu
XM_017016377.2:c.674T>A	XP_016871866.1:p.Val225Glu
XM_017016378.2:c.494T>A	XP_016871867.1:p.Val165Glu
NM_018344.6:c.1112T>A MANE Select	NP_060814.4:p.Val371Glu
NM_001174098.2:c.*341T>A	NP_001167569.1:n.*341T>A
NM_001363518.2:c.878T>A	NP_001350447.1:p.Val293Glu
NR_033413.2:n.1080T>A
NR_033414.2:n.853T>A