Canonical Allele Identifier: CA668072043
Gene: SLC29A3 HGNC NCBI

Linked Data

dbSNP Id: rs1389816017

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71344302C>T , CM000672.2:g.71344302C>T GRCh38
NC_000010.10:g.73104059C>T , CM000672.1:g.73104059C>T GRCh37
NC_000010.9:g.72774065C>T NCBI36
NG_017066.1:g.30050C>T
NG_017066.2:g.30044C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697843.1:n.829+11C>T
ENST00000373189.6:c.383+11C>T MANE Select ENSP00000362285.5:n.383+11C>T
ENST00000479577.2:c.149+11C>T ENSP00000493995.1:n.149+11C>T
ENST00000642198.1:c.67-7260C>T ENSP00000494827.1:n.67-7260C>T
ENST00000642772.1:c.301-11779C>T ENSP00000495041.1:n.301-11779C>T
ENST00000643042.1:c.232-11779C>T ENSP00000496674.1:n.232-11779C>T
ENST00000643619.1:c.149+11C>T ENSP00000494378.1:n.149+11C>T
ENST00000643752.1:c.383+11C>T ENSP00000495000.1:n.383+11C>T
ENST00000644088.1:c.301-11779C>T ENSP00000494066.1:n.301-11779C>T
ENST00000644591.1:c.301-7260C>T ENSP00000496664.1:n.301-7260C>T
ENST00000644895.1:c.301-7260C>T ENSP00000493872.1:n.301-7260C>T
ENST00000645345.1:c.301-7260C>T ENSP00000495859.1:n.301-7260C>T
ENST00000647524.1:c.383+11C>T ENSP00000495077.1:n.383+11C>T
ENST00000373189.5:c.383+11C>T ENSP00000362285.5:n.383+11C>T
NM_001174098.1:c.383+11C>T NP_001167569.1:n.383+11C>T
NM_018344.5:c.383+11C>T NP_060814.4:n.383+11C>T
NR_033413.1:n.358-7260C>T
NR_033414.1:n.358-11779C>T
XM_006717910.2:c.149+11C>T XP_006717973.1:n.149+11C>T
XR_946051.1:n.626-2921G>A
NM_001363518.1:c.149+11C>T NP_001350447.1:n.149+11C>T
XM_017016377.2:c.-55-7260C>T XP_016871866.1:n.-55-7260C>T
XM_017016378.2:c.-8-11779C>T XP_016871867.1:n.-8-11779C>T
XR_001747496.1:n.1552-2921G>A
XR_946051.2:n.1552-2921G>A
NM_018344.6:c.383+11C>T MANE Select NP_060814.4:n.383+11C>T
NM_001174098.2:c.383+11C>T NP_001167569.1:n.383+11C>T
NM_001363518.2:c.149+11C>T NP_001350447.1:n.149+11C>T
NR_033413.2:n.352-7260C>T
NR_033414.2:n.352-11779C>T