Canonical Allele Identifier: CA730462422
Gene: RAB29 HGNC NCBI

Linked Data

dbSNP Id: rs1206220677

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205775284_205775295dup , CM000663.2:g.205775284_205775295dup GRCh38
NC_000001.10:g.205744412_205744423dup , CM000663.1:g.205744412_205744423dup GRCh37
NC_000001.9:g.204011035_204011046dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367139.8:c.-151_-140dup MANE Select ENSP00000356107.3:n.-151_-140dup
ENST00000235932.8:c.-131+81_-131+92dup ENSP00000235932.4:n.-131+81_-131+92dup
ENST00000367139.7:c.-151_-140dup ENSP00000356107.3:n.-151_-140dup
ENST00000414729.1:c.-337_-326dup ENSP00000402910.1:n.-337_-326dup
ENST00000437324.6:c.-113_-102dup ENSP00000416613.2:n.-113_-102dup
ENST00000468887.1:n.148_159dup
ENST00000528078.1:c.-151_-140dup ENSP00000431483.1:n.-151_-140dup
NM_001135662.1:c.-131+81_-131+92dup NP_001129134.1:n.-131+81_-131+92dup
NM_001135663.1:c.-337_-326dup NP_001129135.1:n.-337_-326dup
NM_001135664.1:c.-113_-102dup NP_001129136.1:n.-113_-102dup
NM_003929.2:c.-151_-140dup NP_003920.1:n.-151_-140dup
XM_005245569.1:c.-136+81_-136+92dup XP_005245626.1:n.-136+81_-136+92dup
XM_005245570.1:c.-156_-145dup XP_005245627.1:n.-156_-145dup
XM_005245571.1:c.-131+109_-131+120dup XP_005245628.1:n.-131+109_-131+120dup
XM_006711605.2:c.-93+81_-93+92dup XP_006711668.1:n.-93+81_-93+92dup
XM_006711606.1:c.-93+109_-93+120dup XP_006711669.1:n.-93+109_-93+120dup
XM_006711605.3:c.-93+81_-93+92dup XP_006711668.1:n.-93+81_-93+92dup
XM_006711606.3:c.-93+109_-93+120dup XP_006711669.1:n.-93+109_-93+120dup
XM_017002748.1:c.-151_-140dup XP_016858237.1:n.-151_-140dup
XM_017002749.1:c.-156_-145dup XP_016858238.1:n.-156_-145dup
XM_017002750.1:c.-131+81_-131+92dup XP_016858239.1:n.-131+81_-131+92dup
NM_003929.3:c.-151_-140dup MANE Select NP_003920.1:n.-151_-140dup
NM_001135662.2:c.-131+81_-131+92dup NP_001129134.1:n.-131+81_-131+92dup
NM_001135663.2:c.-337_-326dup NP_001129135.1:n.-337_-326dup
NM_001135664.2:c.-113_-102dup NP_001129136.1:n.-113_-102dup