Canonical Allele Identifier: CA2609557438
Gene: SLC29A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71344131del , CM000672.2:g.71344131del GRCh38
NC_000010.10:g.73103888del , CM000672.1:g.73103888del GRCh37
NC_000010.9:g.72773894del NCBI36
NG_017066.1:g.29879del
NG_017066.2:g.29873del

Transcript Alleles

HGVS Amino-acid change
ENST00000697843.1:n.747-78del
ENST00000373189.6:c.301-78del MANE Select ENSP00000362285.5:n.301-78del
ENST00000479577.2:c.67-78del ENSP00000493995.1:n.67-78del
ENST00000642198.1:c.67-7431del ENSP00000494827.1:n.67-7431del
ENST00000642772.1:c.301-11950del ENSP00000495041.1:n.301-11950del
ENST00000643042.1:c.232-11950del ENSP00000496674.1:n.232-11950del
ENST00000643619.1:c.67-78del ENSP00000494378.1:n.67-78del
ENST00000643752.1:c.301-78del ENSP00000495000.1:n.301-78del
ENST00000644088.1:c.301-11950del ENSP00000494066.1:n.301-11950del
ENST00000644591.1:c.301-7431del ENSP00000496664.1:n.301-7431del
ENST00000644895.1:c.301-7431del ENSP00000493872.1:n.301-7431del
ENST00000645345.1:c.301-7431del ENSP00000495859.1:n.301-7431del
ENST00000647524.1:c.301-78del ENSP00000495077.1:n.301-78del
ENST00000373189.5:c.301-78del ENSP00000362285.5:n.301-78del
NM_001174098.1:c.301-78del NP_001167569.1:n.301-78del
NM_018344.5:c.301-78del NP_060814.4:n.301-78del
NR_033413.1:n.358-7431del
NR_033414.1:n.358-11950del
XM_006717910.2:c.67-78del XP_006717973.1:n.67-78del
XR_946051.1:n.626-2747del
NM_001363518.1:c.67-78del NP_001350447.1:n.67-78del
XM_017016377.2:c.-55-7431del XP_016871866.1:n.-55-7431del
XM_017016378.2:c.-8-11950del XP_016871867.1:n.-8-11950del
XR_001747496.1:n.1552-2747del
XR_001747497.1:n.82+34del
XR_946051.2:n.1552-2747del
NM_018344.6:c.301-78del MANE Select NP_060814.4:n.301-78del
NM_001174098.2:c.301-78del NP_001167569.1:n.301-78del
NM_001363518.2:c.67-78del NP_001350447.1:n.67-78del
NR_033413.2:n.352-7431del
NR_033414.2:n.352-11950del