Canonical Allele Identifier: CA377117291

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122259T>C (hg19) ; chr10:g.71362502T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362502T>C , CM000672.2:g.71362502T>C	GRCh38
NC_000010.10:g.73122259T>C , CM000672.1:g.73122259T>C	GRCh37
NC_000010.9:g.72792265T>C	NCBI36
NG_017066.1:g.48250T>C
NG_017066.2:g.48244T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000697843.1:n.2798T>C
ENST00000373189.6:c.1322T>C MANE Select	ENSP00000362285.5:p.Val441Ala
ENST00000479577.2:c.1088T>C	ENSP00000493995.1:p.Val363Ala
ENST00000642198.1:c.*894T>C	ENSP00000494827.1:n.*894T>C
ENST00000642772.1:c.*94+6259T>C	ENSP00000495041.1:n.*94+6259T>C
ENST00000643042.1:c.943T>C	ENSP00000496674.1:n.943T>C
ENST00000643619.1:c.*905T>C	ENSP00000494378.1:n.*905T>C
ENST00000643752.1:c.*648T>C	ENSP00000495000.1:n.*648T>C
ENST00000644088.1:c.*643T>C	ENSP00000494066.1:n.*643T>C
ENST00000644591.1:c.*648T>C	ENSP00000496664.1:n.*648T>C
ENST00000644895.1:c.*99+6259T>C	ENSP00000493872.1:n.*99+6259T>C
ENST00000645345.1:c.*894T>C	ENSP00000495859.1:n.*894T>C
ENST00000647524.1:c.*905T>C	ENSP00000495077.1:n.*905T>C
ENST00000373189.5:c.1322T>C	ENSP00000362285.5:p.Val441Ala
ENST00000469204.1:n.819T>C
NM_001174098.1:c.*551T>C	NP_001167569.1:n.*551T>C
NM_018344.5:c.1322T>C	NP_060814.4:p.Val441Ala
NR_033413.1:n.1296T>C
NR_033414.1:n.1069T>C
XM_006717910.2:c.1088T>C	XP_006717973.1:p.Val363Ala
NM_001363518.1:c.1088T>C	NP_001350447.1:p.Val363Ala
XM_017016377.2:c.884T>C	XP_016871866.1:p.Val295Ala
XM_017016378.2:c.704T>C	XP_016871867.1:p.Val235Ala
NM_018344.6:c.1322T>C MANE Select	NP_060814.4:p.Val441Ala
NM_001174098.2:c.*551T>C	NP_001167569.1:n.*551T>C
NM_001363518.2:c.1088T>C	NP_001350447.1:p.Val363Ala
NR_033413.2:n.1290T>C
NR_033414.2:n.1063T>C