Canonical Allele Identifier: CA470281185

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121921C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362164C>G , CM000672.2:g.71362164C>G	GRCh38
NC_000010.10:g.73121921C>G , CM000672.1:g.73121921C>G	GRCh37
NC_000010.9:g.72791927C>G	NCBI36
NG_017066.1:g.47912C>G
NG_017066.2:g.47906C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2460C>G
ENST00000373189.6:c.984C>G MANE Select	ENSP00000362285.5:p.Thr328=
ENST00000479577.2:c.750C>G	ENSP00000493995.1:p.Thr250=
ENST00000642198.1:c.*556C>G	ENSP00000494827.1:n.*556C>G
ENST00000642772.1:c.*94+5921C>G	ENSP00000495041.1:n.*94+5921C>G
ENST00000643042.1:c.605C>G	ENSP00000496674.1:n.605C>G
ENST00000643619.1:c.*567C>G	ENSP00000494378.1:n.*567C>G
ENST00000643752.1:c.*310C>G	ENSP00000495000.1:n.*310C>G
ENST00000644088.1:c.*305C>G	ENSP00000494066.1:n.*305C>G
ENST00000644591.1:c.*310C>G	ENSP00000496664.1:n.*310C>G
ENST00000644895.1:c.*99+5921C>G	ENSP00000493872.1:n.*99+5921C>G
ENST00000645345.1:c.*556C>G	ENSP00000495859.1:n.*556C>G
ENST00000647524.1:c.*567C>G	ENSP00000495077.1:n.*567C>G
ENST00000373189.5:c.984C>G	ENSP00000362285.5:p.Thr328=
ENST00000469204.1:n.481C>G
NM_001174098.1:c.*213C>G	NP_001167569.1:n.*213C>G
NM_018344.5:c.984C>G	NP_060814.4:p.Thr328=
NR_033413.1:n.958C>G
NR_033414.1:n.731C>G
XM_006717910.2:c.750C>G	XP_006717973.1:p.Thr250=
NM_001363518.1:c.750C>G	NP_001350447.1:p.Thr250=
XM_017016377.2:c.546C>G	XP_016871866.1:p.Thr182=
XM_017016378.2:c.366C>G	XP_016871867.1:p.Thr122=
NM_018344.6:c.984C>G MANE Select	NP_060814.4:p.Thr328=
NM_001174098.2:c.*213C>G	NP_001167569.1:n.*213C>G
NM_001363518.2:c.750C>G	NP_001350447.1:p.Thr250=
NR_033413.2:n.952C>G
NR_033414.2:n.725C>G