Canonical Allele Identifier: CA646373503
Gene: RAB29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205775336_205775337insC , CM000663.2:g.205775336_205775337insC GRCh38
NC_000001.10:g.205744464_205744465insC , CM000663.1:g.205744464_205744465insC GRCh37
NC_000001.9:g.204011087_204011088insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367139.8:c.-195_-194insG MANE Select ENSP00000356107.3:n.-195_-194insG
ENST00000235932.8:c.-131+37_-131+38insG ENSP00000235932.4:n.-131+37_-131+38insG
ENST00000367139.7:c.-195_-194insG ENSP00000356107.3:n.-195_-194insG
ENST00000414729.1:c.-381_-380insG ENSP00000402910.1:n.-381_-380insG
ENST00000437324.6:c.-157_-156insG ENSP00000416613.2:n.-157_-156insG
ENST00000468887.1:n.104_105insG
ENST00000528078.1:c.-195_-194insG ENSP00000431483.1:n.-195_-194insG
NM_001135662.1:c.-131+37_-131+38insG NP_001129134.1:n.-131+37_-131+38insG
NM_001135663.1:c.-381_-380insG NP_001129135.1:n.-381_-380insG
NM_001135664.1:c.-157_-156insG NP_001129136.1:n.-157_-156insG
NM_003929.2:c.-195_-194insG NP_003920.1:n.-195_-194insG
XM_005245569.1:c.-136+37_-136+38insG XP_005245626.1:n.-136+37_-136+38insG
XM_005245570.1:c.-200_-199insG XP_005245627.1:n.-200_-199insG
XM_005245571.1:c.-131+65_-131+66insG XP_005245628.1:n.-131+65_-131+66insG
XM_006711605.2:c.-93+37_-93+38insG XP_006711668.1:n.-93+37_-93+38insG
XM_006711606.1:c.-93+65_-93+66insG XP_006711669.1:n.-93+65_-93+66insG
XM_006711605.3:c.-93+37_-93+38insG XP_006711668.1:n.-93+37_-93+38insG
XM_006711606.3:c.-93+65_-93+66insG XP_006711669.1:n.-93+65_-93+66insG
XM_017002748.1:c.-195_-194insG XP_016858237.1:n.-195_-194insG
XM_017002749.1:c.-200_-199insG XP_016858238.1:n.-200_-199insG
XM_017002750.1:c.-131+37_-131+38insG XP_016858239.1:n.-131+37_-131+38insG
NM_003929.3:c.-195_-194insG MANE Select NP_003920.1:n.-195_-194insG
NM_001135662.2:c.-131+37_-131+38insG NP_001129134.1:n.-131+37_-131+38insG
NM_001135663.2:c.-381_-380insG NP_001129135.1:n.-381_-380insG
NM_001135664.2:c.-157_-156insG NP_001129136.1:n.-157_-156insG