Canonical Allele Identifier: CA470281119

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121882C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362125C>G , CM000672.2:g.71362125C>G	GRCh38
NC_000010.10:g.73121882C>G , CM000672.1:g.73121882C>G	GRCh37
NC_000010.9:g.72791888C>G	NCBI36
NG_017066.1:g.47873C>G
NG_017066.2:g.47867C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2421C>G
ENST00000373189.6:c.945C>G MANE Select	ENSP00000362285.5:p.Val315=
ENST00000479577.2:c.711C>G	ENSP00000493995.1:p.Val237=
ENST00000642198.1:c.*517C>G	ENSP00000494827.1:n.*517C>G
ENST00000642772.1:c.*94+5882C>G	ENSP00000495041.1:n.*94+5882C>G
ENST00000643042.1:c.566C>G	ENSP00000496674.1:n.566C>G
ENST00000643619.1:c.*528C>G	ENSP00000494378.1:n.*528C>G
ENST00000643752.1:c.*271C>G	ENSP00000495000.1:n.*271C>G
ENST00000644088.1:c.*266C>G	ENSP00000494066.1:n.*266C>G
ENST00000644591.1:c.*271C>G	ENSP00000496664.1:n.*271C>G
ENST00000644895.1:c.*99+5882C>G	ENSP00000493872.1:n.*99+5882C>G
ENST00000645345.1:c.*517C>G	ENSP00000495859.1:n.*517C>G
ENST00000647524.1:c.*528C>G	ENSP00000495077.1:n.*528C>G
ENST00000373189.5:c.945C>G	ENSP00000362285.5:p.Val315=
ENST00000469204.1:n.442C>G
NM_001174098.1:c.*174C>G	NP_001167569.1:n.*174C>G
NM_018344.5:c.945C>G	NP_060814.4:p.Val315=
NR_033413.1:n.919C>G
NR_033414.1:n.692C>G
XM_006717910.2:c.711C>G	XP_006717973.1:p.Val237=
NM_001363518.1:c.711C>G	NP_001350447.1:p.Val237=
XM_017016377.2:c.507C>G	XP_016871866.1:p.Val169=
XM_017016378.2:c.327C>G	XP_016871867.1:p.Val109=
NM_018344.6:c.945C>G MANE Select	NP_060814.4:p.Val315=
NM_001174098.2:c.*174C>G	NP_001167569.1:n.*174C>G
NM_001363518.2:c.711C>G	NP_001350447.1:p.Val237=
NR_033413.2:n.913C>G
NR_033414.2:n.686C>G