Canonical Allele Identifier: CA470281315

Gene: SLC29A3

Linked Data

• MyVariant Identifiers: chr10:g.73122098C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71362341C>T , CM000672.2:g.71362341C>T	GRCh38
NC_000010.10:g.73122098C>T , CM000672.1:g.73122098C>T	GRCh37
NC_000010.9:g.72792104C>T	NCBI36
NG_017066.1:g.48089C>T
NG_017066.2:g.48083C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697843.1:n.2637C>T
ENST00000373189.6:c.1161C>T MANE Select	ENSP00000362285.5:p.Thr387=
ENST00000479577.2:c.927C>T	ENSP00000493995.1:p.Thr309=
ENST00000642198.1:c.*733C>T	ENSP00000494827.1:n.*733C>T
ENST00000642772.1:c.*94+6098C>T	ENSP00000495041.1:n.*94+6098C>T
ENST00000643042.1:c.782C>T	ENSP00000496674.1:n.782C>T
ENST00000643619.1:c.*744C>T	ENSP00000494378.1:n.*744C>T
ENST00000643752.1:c.*487C>T	ENSP00000495000.1:n.*487C>T
ENST00000644088.1:c.*482C>T	ENSP00000494066.1:n.*482C>T
ENST00000644591.1:c.*487C>T	ENSP00000496664.1:n.*487C>T
ENST00000644895.1:c.*99+6098C>T	ENSP00000493872.1:n.*99+6098C>T
ENST00000645345.1:c.*733C>T	ENSP00000495859.1:n.*733C>T
ENST00000647524.1:c.*744C>T	ENSP00000495077.1:n.*744C>T
ENST00000373189.5:c.1161C>T	ENSP00000362285.5:p.Thr387=
ENST00000469204.1:n.658C>T
NM_001174098.1:c.*390C>T	NP_001167569.1:n.*390C>T
NM_018344.5:c.1161C>T	NP_060814.4:p.Thr387=
NR_033413.1:n.1135C>T
NR_033414.1:n.908C>T
XM_006717910.2:c.927C>T	XP_006717973.1:p.Thr309=
NM_001363518.1:c.927C>T	NP_001350447.1:p.Thr309=
XM_017016377.2:c.723C>T	XP_016871866.1:p.Thr241=
XM_017016378.2:c.543C>T	XP_016871867.1:p.Thr181=
NM_018344.6:c.1161C>T MANE Select	NP_060814.4:p.Thr387=
NM_001174098.2:c.*390C>T	NP_001167569.1:n.*390C>T
NM_001363518.2:c.927C>T	NP_001350447.1:p.Thr309=
NR_033413.2:n.1129C>T
NR_033414.2:n.902C>T