Canonical Allele Identifier: CA470281650

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122287A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362530A>G , CM000672.2:g.71362530A>G	GRCh38
NC_000010.10:g.73122287A>G , CM000672.1:g.73122287A>G	GRCh37
NC_000010.9:g.72792293A>G	NCBI36
NG_017066.1:g.48278A>G
NG_017066.2:g.48272A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2826A>G
ENST00000373189.6:c.1350A>G MANE Select	ENSP00000362285.5:p.Gly450=
ENST00000479577.2:c.1116A>G	ENSP00000493995.1:p.Gly372=
ENST00000642198.1:c.*922A>G	ENSP00000494827.1:n.*922A>G
ENST00000642772.1:c.*94+6287A>G	ENSP00000495041.1:n.*94+6287A>G
ENST00000643042.1:c.971A>G	ENSP00000496674.1:n.971A>G
ENST00000643619.1:c.*933A>G	ENSP00000494378.1:n.*933A>G
ENST00000643752.1:c.*676A>G	ENSP00000495000.1:n.*676A>G
ENST00000644088.1:c.*671A>G	ENSP00000494066.1:n.*671A>G
ENST00000644591.1:c.*676A>G	ENSP00000496664.1:n.*676A>G
ENST00000644895.1:c.*99+6287A>G	ENSP00000493872.1:n.*99+6287A>G
ENST00000645345.1:c.*922A>G	ENSP00000495859.1:n.*922A>G
ENST00000647524.1:c.*933A>G	ENSP00000495077.1:n.*933A>G
ENST00000373189.5:c.1350A>G	ENSP00000362285.5:p.Gly450=
NM_001174098.1:c.*579A>G	NP_001167569.1:n.*579A>G
NM_018344.5:c.1350A>G	NP_060814.4:p.Gly450=
NR_033413.1:n.1324A>G
NR_033414.1:n.1097A>G
XM_006717910.2:c.1116A>G	XP_006717973.1:p.Gly372=
NM_001363518.1:c.1116A>G	NP_001350447.1:p.Gly372=
XM_017016377.2:c.912A>G	XP_016871866.1:p.Gly304=
XM_017016378.2:c.732A>G	XP_016871867.1:p.Gly244=
NM_018344.6:c.1350A>G MANE Select	NP_060814.4:p.Gly450=
NM_001174098.2:c.*579A>G	NP_001167569.1:n.*579A>G
NM_001363518.2:c.1116A>G	NP_001350447.1:p.Gly372=
NR_033413.2:n.1318A>G
NR_033414.2:n.1091A>G