Canonical Allele Identifier: CA377117073

Gene: SLC29A3

Linked Data

• dbSNP Id: rs1847087509
• MyVariant Identifiers: chr10:g.73122160T>C (hg19) ; chr10:g.71362403T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362403T>C , CM000672.2:g.71362403T>C	GRCh38
NC_000010.10:g.73122160T>C , CM000672.1:g.73122160T>C	GRCh37
NC_000010.9:g.72792166T>C	NCBI36
NG_017066.1:g.48151T>C
NG_017066.2:g.48145T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2699T>C
ENST00000373189.6:c.1223T>C MANE Select	ENSP00000362285.5:p.Val408Ala
ENST00000479577.2:c.989T>C	ENSP00000493995.1:p.Val330Ala
ENST00000642198.1:c.*795T>C	ENSP00000494827.1:n.*795T>C
ENST00000642772.1:c.*94+6160T>C	ENSP00000495041.1:n.*94+6160T>C
ENST00000643042.1:c.844T>C	ENSP00000496674.1:n.844T>C
ENST00000643619.1:c.*806T>C	ENSP00000494378.1:n.*806T>C
ENST00000643752.1:c.*549T>C	ENSP00000495000.1:n.*549T>C
ENST00000644088.1:c.*544T>C	ENSP00000494066.1:n.*544T>C
ENST00000644591.1:c.*549T>C	ENSP00000496664.1:n.*549T>C
ENST00000644895.1:c.*99+6160T>C	ENSP00000493872.1:n.*99+6160T>C
ENST00000645345.1:c.*795T>C	ENSP00000495859.1:n.*795T>C
ENST00000647524.1:c.*806T>C	ENSP00000495077.1:n.*806T>C
ENST00000373189.5:c.1223T>C	ENSP00000362285.5:p.Val408Ala
ENST00000469204.1:n.720T>C
NM_001174098.1:c.*452T>C	NP_001167569.1:n.*452T>C
NM_018344.5:c.1223T>C	NP_060814.4:p.Val408Ala
NR_033413.1:n.1197T>C
NR_033414.1:n.970T>C
XM_006717910.2:c.989T>C	XP_006717973.1:p.Val330Ala
NM_001363518.1:c.989T>C	NP_001350447.1:p.Val330Ala
XM_017016377.2:c.785T>C	XP_016871866.1:p.Val262Ala
XM_017016378.2:c.605T>C	XP_016871867.1:p.Val202Ala
NM_018344.6:c.1223T>C MANE Select	NP_060814.4:p.Val408Ala
NM_001174098.2:c.*452T>C	NP_001167569.1:n.*452T>C
NM_001363518.2:c.989T>C	NP_001350447.1:p.Val330Ala
NR_033413.2:n.1191T>C
NR_033414.2:n.964T>C