Canonical Allele Identifier: CA2650149899
Gene: RAB29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205775003_205775009del , CM000663.2:g.205775003_205775009del GRCh38
NC_000001.10:g.205744131_205744137del , CM000663.1:g.205744131_205744137del GRCh37
NC_000001.9:g.204010754_204010760del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367139.8:c.-47_-41del MANE Select ENSP00000356107.3:n.-47_-41del
ENST00000235932.8:c.-47_-41del ENSP00000235932.4:n.-47_-41del
ENST00000367139.7:c.-47_-41del ENSP00000356107.3:n.-47_-41del
ENST00000414729.1:c.-47_-41del ENSP00000402910.1:n.-47_-41del
ENST00000437324.6:c.-93+270_-93+276del ENSP00000416613.2:n.-93+270_-93+276del
ENST00000446390.6:c.-47_-41del ENSP00000389899.2:n.-47_-41del
ENST00000468887.1:n.168+270_168+276del
ENST00000492534.1:n.149_155del
ENST00000528078.1:c.-47_-41del ENSP00000431483.1:n.-47_-41del
ENST00000533111.1:n.81+126_81+132del
NM_001135662.1:c.-47_-41del NP_001129134.1:n.-47_-41del
NM_001135663.1:c.-47_-41del NP_001129135.1:n.-47_-41del
NM_001135664.1:c.-93+270_-93+276del NP_001129136.1:n.-93+270_-93+276del
NM_003929.2:c.-47_-41del NP_003920.1:n.-47_-41del
XM_005245569.1:c.-47_-41del XP_005245626.1:n.-47_-41del
XM_005245570.1:c.-47_-41del XP_005245627.1:n.-47_-41del
XM_005245571.1:c.-47_-41del XP_005245628.1:n.-47_-41del
XM_006711605.2:c.-93+371_-93+377del XP_006711668.1:n.-93+371_-93+377del
XM_006711606.1:c.-93+399_-93+405del XP_006711669.1:n.-93+399_-93+405del
XM_006711605.3:c.-93+371_-93+377del XP_006711668.1:n.-93+371_-93+377del
XM_006711606.3:c.-93+399_-93+405del XP_006711669.1:n.-93+399_-93+405del
XM_017002748.1:c.-47_-41del XP_016858237.1:n.-47_-41del
XM_017002749.1:c.-47_-41del XP_016858238.1:n.-47_-41del
XM_017002750.1:c.-47_-41del XP_016858239.1:n.-47_-41del
NM_003929.3:c.-47_-41del MANE Select NP_003920.1:n.-47_-41del
NM_001135662.2:c.-47_-41del NP_001129134.1:n.-47_-41del
NM_001135663.2:c.-47_-41del NP_001129135.1:n.-47_-41del
NM_001135664.2:c.-93+270_-93+276del NP_001129136.1:n.-93+270_-93+276del