Canonical Allele Identifier: CA470281140

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73121891C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362134C>T , CM000672.2:g.71362134C>T	GRCh38
NC_000010.10:g.73121891C>T , CM000672.1:g.73121891C>T	GRCh37
NC_000010.9:g.72791897C>T	NCBI36
NG_017066.1:g.47882C>T
NG_017066.2:g.47876C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2430C>T
ENST00000373189.6:c.954C>T MANE Select	ENSP00000362285.5:p.Ile318=
ENST00000479577.2:c.720C>T	ENSP00000493995.1:p.Ile240=
ENST00000642198.1:c.*526C>T	ENSP00000494827.1:n.*526C>T
ENST00000642772.1:c.*94+5891C>T	ENSP00000495041.1:n.*94+5891C>T
ENST00000643042.1:c.575C>T	ENSP00000496674.1:n.575C>T
ENST00000643619.1:c.*537C>T	ENSP00000494378.1:n.*537C>T
ENST00000643752.1:c.*280C>T	ENSP00000495000.1:n.*280C>T
ENST00000644088.1:c.*275C>T	ENSP00000494066.1:n.*275C>T
ENST00000644591.1:c.*280C>T	ENSP00000496664.1:n.*280C>T
ENST00000644895.1:c.*99+5891C>T	ENSP00000493872.1:n.*99+5891C>T
ENST00000645345.1:c.*526C>T	ENSP00000495859.1:n.*526C>T
ENST00000647524.1:c.*537C>T	ENSP00000495077.1:n.*537C>T
ENST00000373189.5:c.954C>T	ENSP00000362285.5:p.Ile318=
ENST00000469204.1:n.451C>T
NM_001174098.1:c.*183C>T	NP_001167569.1:n.*183C>T
NM_018344.5:c.954C>T	NP_060814.4:p.Ile318=
NR_033413.1:n.928C>T
NR_033414.1:n.701C>T
XM_006717910.2:c.720C>T	XP_006717973.1:p.Ile240=
NM_001363518.1:c.720C>T	NP_001350447.1:p.Ile240=
XM_017016377.2:c.516C>T	XP_016871866.1:p.Ile172=
XM_017016378.2:c.336C>T	XP_016871867.1:p.Ile112=
NM_018344.6:c.954C>T MANE Select	NP_060814.4:p.Ile318=
NM_001174098.2:c.*183C>T	NP_001167569.1:n.*183C>T
NM_001363518.2:c.720C>T	NP_001350447.1:p.Ile240=
NR_033413.2:n.922C>T
NR_033414.2:n.695C>T