Canonical Allele Identifier: CA470281383

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122137C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362380C>T , CM000672.2:g.71362380C>T	GRCh38
NC_000010.10:g.73122137C>T , CM000672.1:g.73122137C>T	GRCh37
NC_000010.9:g.72792143C>T	NCBI36
NG_017066.1:g.48128C>T
NG_017066.2:g.48122C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2676C>T
ENST00000373189.6:c.1200C>T MANE Select	ENSP00000362285.5:p.Pro400=
ENST00000479577.2:c.966C>T	ENSP00000493995.1:p.Pro322=
ENST00000642198.1:c.*772C>T	ENSP00000494827.1:n.*772C>T
ENST00000642772.1:c.*94+6137C>T	ENSP00000495041.1:n.*94+6137C>T
ENST00000643042.1:c.821C>T	ENSP00000496674.1:n.821C>T
ENST00000643619.1:c.*783C>T	ENSP00000494378.1:n.*783C>T
ENST00000643752.1:c.*526C>T	ENSP00000495000.1:n.*526C>T
ENST00000644088.1:c.*521C>T	ENSP00000494066.1:n.*521C>T
ENST00000644591.1:c.*526C>T	ENSP00000496664.1:n.*526C>T
ENST00000644895.1:c.*99+6137C>T	ENSP00000493872.1:n.*99+6137C>T
ENST00000645345.1:c.*772C>T	ENSP00000495859.1:n.*772C>T
ENST00000647524.1:c.*783C>T	ENSP00000495077.1:n.*783C>T
ENST00000373189.5:c.1200C>T	ENSP00000362285.5:p.Pro400=
ENST00000469204.1:n.697C>T
NM_001174098.1:c.*429C>T	NP_001167569.1:n.*429C>T
NM_018344.5:c.1200C>T	NP_060814.4:p.Pro400=
NR_033413.1:n.1174C>T
NR_033414.1:n.947C>T
XM_006717910.2:c.966C>T	XP_006717973.1:p.Pro322=
NM_001363518.1:c.966C>T	NP_001350447.1:p.Pro322=
XM_017016377.2:c.762C>T	XP_016871866.1:p.Pro254=
XM_017016378.2:c.582C>T	XP_016871867.1:p.Pro194=
NM_018344.6:c.1200C>T MANE Select	NP_060814.4:p.Pro400=
NM_001174098.2:c.*429C>T	NP_001167569.1:n.*429C>T
NM_001363518.2:c.966C>T	NP_001350447.1:p.Pro322=
NR_033413.2:n.1168C>T
NR_033414.2:n.941C>T