Canonical Allele Identifier: CA2650150058
Gene: RAB29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205775062_205775063del , CM000663.2:g.205775062_205775063del GRCh38
NC_000001.10:g.205744190_205744191del , CM000663.1:g.205744190_205744191del GRCh37
NC_000001.9:g.204010813_204010814del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367139.8:c.-107_-106del MANE Select ENSP00000356107.3:n.-107_-106del
ENST00000235932.8:c.-107_-106del ENSP00000235932.4:n.-107_-106del
ENST00000367139.7:c.-107_-106del ENSP00000356107.3:n.-107_-106del
ENST00000414729.1:c.-107_-106del ENSP00000402910.1:n.-107_-106del
ENST00000437324.6:c.-93+210_-93+211del ENSP00000416613.2:n.-93+210_-93+211del
ENST00000446390.6:c.-107_-106del ENSP00000389899.2:n.-107_-106del
ENST00000468887.1:n.168+210_168+211del
ENST00000492534.1:n.89_90del
ENST00000528078.1:c.-107_-106del ENSP00000431483.1:n.-107_-106del
ENST00000533111.1:n.81+66_81+67del
NM_001135662.1:c.-107_-106del NP_001129134.1:n.-107_-106del
NM_001135663.1:c.-107_-106del NP_001129135.1:n.-107_-106del
NM_001135664.1:c.-93+210_-93+211del NP_001129136.1:n.-93+210_-93+211del
NM_003929.2:c.-107_-106del NP_003920.1:n.-107_-106del
XM_005245569.1:c.-107_-106del XP_005245626.1:n.-107_-106del
XM_005245570.1:c.-107_-106del XP_005245627.1:n.-107_-106del
XM_005245571.1:c.-107_-106del XP_005245628.1:n.-107_-106del
XM_006711605.2:c.-93+311_-93+312del XP_006711668.1:n.-93+311_-93+312del
XM_006711606.1:c.-93+339_-93+340del XP_006711669.1:n.-93+339_-93+340del
XM_006711605.3:c.-93+311_-93+312del XP_006711668.1:n.-93+311_-93+312del
XM_006711606.3:c.-93+339_-93+340del XP_006711669.1:n.-93+339_-93+340del
XM_017002748.1:c.-107_-106del XP_016858237.1:n.-107_-106del
XM_017002749.1:c.-107_-106del XP_016858238.1:n.-107_-106del
XM_017002750.1:c.-107_-106del XP_016858239.1:n.-107_-106del
NM_003929.3:c.-107_-106del MANE Select NP_003920.1:n.-107_-106del
NM_001135662.2:c.-107_-106del NP_001129134.1:n.-107_-106del
NM_001135663.2:c.-107_-106del NP_001129135.1:n.-107_-106del
NM_001135664.2:c.-93+210_-93+211del NP_001129136.1:n.-93+210_-93+211del