Canonical Allele Identifier: CA377114443

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121819C>A (hg19) ; chr10:g.71362062C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362062C>A , CM000672.2:g.71362062C>A	GRCh38
NC_000010.10:g.73121819C>A , CM000672.1:g.73121819C>A	GRCh37
NC_000010.9:g.72791825C>A	NCBI36
NG_017066.1:g.47810C>A
NG_017066.2:g.47804C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2358C>A
ENST00000373189.6:c.882C>A MANE Select	ENSP00000362285.5:p.His294Gln
ENST00000479577.2:c.648C>A	ENSP00000493995.1:p.His216Gln
ENST00000642198.1:c.*454C>A	ENSP00000494827.1:n.*454C>A
ENST00000642772.1:c.*94+5819C>A	ENSP00000495041.1:n.*94+5819C>A
ENST00000643042.1:c.503C>A	ENSP00000496674.1:n.503C>A
ENST00000643619.1:c.*465C>A	ENSP00000494378.1:n.*465C>A
ENST00000643752.1:c.*208C>A	ENSP00000495000.1:n.*208C>A
ENST00000644088.1:c.*203C>A	ENSP00000494066.1:n.*203C>A
ENST00000644591.1:c.*208C>A	ENSP00000496664.1:n.*208C>A
ENST00000644895.1:c.*99+5819C>A	ENSP00000493872.1:n.*99+5819C>A
ENST00000645345.1:c.*454C>A	ENSP00000495859.1:n.*454C>A
ENST00000647524.1:c.*465C>A	ENSP00000495077.1:n.*465C>A
ENST00000373189.5:c.882C>A	ENSP00000362285.5:p.His294Gln
ENST00000469204.1:n.379C>A
NM_001174098.1:c.*111C>A	NP_001167569.1:n.*111C>A
NM_018344.5:c.882C>A	NP_060814.4:p.His294Gln
NR_033413.1:n.856C>A
NR_033414.1:n.629C>A
XM_006717910.2:c.648C>A	XP_006717973.1:p.His216Gln
NM_001363518.1:c.648C>A	NP_001350447.1:p.His216Gln
XM_017016377.2:c.444C>A	XP_016871866.1:p.His148Gln
XM_017016378.2:c.264C>A	XP_016871867.1:p.His88Gln
NM_018344.6:c.882C>A MANE Select	NP_060814.4:p.His294Gln
NM_001174098.2:c.*111C>A	NP_001167569.1:n.*111C>A
NM_001363518.2:c.648C>A	NP_001350447.1:p.His216Gln
NR_033413.2:n.850C>A
NR_033414.2:n.623C>A