Canonical Allele Identifier: CA2482718087
Gene: RAB29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205775242_205775243delinsAC , CM000663.2:g.205775242_205775243delinsAC GRCh38
NC_000001.10:g.205744370_205744371delinsAC , CM000663.1:g.205744370_205744371delinsAC GRCh37
NC_000001.9:g.204010993_204010994delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367139.8:c.-131+30_-131+31delinsGT MANE Select ENSP00000356107.3:n.-131+30_-131+31delinsGT
ENST00000235932.8:c.-131+131_-131+132delinsGT ENSP00000235932.4:n.-131+131_-131+132delinsGT
ENST00000367139.7:c.-131+30_-131+31delinsGT ENSP00000356107.3:n.-131+30_-131+31delinsGT
ENST00000414729.1:c.-287_-286delinsGT ENSP00000402910.1:n.-287_-286delinsGT
ENST00000437324.6:c.-93+30_-93+31delinsGT ENSP00000416613.2:n.-93+30_-93+31delinsGT
ENST00000468887.1:n.168+30_168+31delinsGT
ENST00000528078.1:c.-131+30_-131+31delinsGT ENSP00000431483.1:n.-131+30_-131+31delinsGT
NM_001135662.1:c.-131+131_-131+132delinsGT NP_001129134.1:n.-131+131_-131+132delinsGT
NM_001135663.1:c.-287_-286delinsGT NP_001129135.1:n.-287_-286delinsGT
NM_001135664.1:c.-93+30_-93+31delinsGT NP_001129136.1:n.-93+30_-93+31delinsGT
NM_003929.2:c.-131+30_-131+31delinsGT NP_003920.1:n.-131+30_-131+31delinsGT
XM_005245569.1:c.-136+131_-136+132delinsGT XP_005245626.1:n.-136+131_-136+132delinsGT
XM_005245570.1:c.-136+30_-136+31delinsGT XP_005245627.1:n.-136+30_-136+31delinsGT
XM_005245571.1:c.-130-157_-130-156delinsGT XP_005245628.1:n.-130-157_-130-156delinsGT
XM_006711605.2:c.-93+131_-93+132delinsGT XP_006711668.1:n.-93+131_-93+132delinsGT
XM_006711606.1:c.-93+159_-93+160delinsGT XP_006711669.1:n.-93+159_-93+160delinsGT
XM_006711605.3:c.-93+131_-93+132delinsGT XP_006711668.1:n.-93+131_-93+132delinsGT
XM_006711606.3:c.-93+159_-93+160delinsGT XP_006711669.1:n.-93+159_-93+160delinsGT
XM_017002748.1:c.-131+30_-131+31delinsGT XP_016858237.1:n.-131+30_-131+31delinsGT
XM_017002749.1:c.-136+30_-136+31delinsGT XP_016858238.1:n.-136+30_-136+31delinsGT
XM_017002750.1:c.-131+131_-131+132delinsGT XP_016858239.1:n.-131+131_-131+132delinsGT
NM_003929.3:c.-131+30_-131+31delinsGT MANE Select NP_003920.1:n.-131+30_-131+31delinsGT
NM_001135662.2:c.-131+131_-131+132delinsGT NP_001129134.1:n.-131+131_-131+132delinsGT
NM_001135663.2:c.-287_-286delinsGT NP_001129135.1:n.-287_-286delinsGT
NM_001135664.2:c.-93+30_-93+31delinsGT NP_001129136.1:n.-93+30_-93+31delinsGT