Canonical Allele Identifier: CA646373528
Gene: RAB29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205775363_205775364insT , CM000663.2:g.205775363_205775364insT GRCh38
NC_000001.10:g.205744491_205744492insT , CM000663.1:g.205744491_205744492insT GRCh37
NC_000001.9:g.204011114_204011115insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367139.8:c.-222_-221insA MANE Select ENSP00000356107.3:n.-222_-221insA
ENST00000235932.8:c.-131+10_-131+11insA ENSP00000235932.4:n.-131+10_-131+11insA
ENST00000367139.7:c.-222_-221insA ENSP00000356107.3:n.-222_-221insA
ENST00000414729.1:c.-408_-407insA ENSP00000402910.1:n.-408_-407insA
ENST00000437324.6:c.-184_-183insA ENSP00000416613.2:n.-184_-183insA
ENST00000468887.1:n.77_78insA
ENST00000528078.1:c.-222_-221insA ENSP00000431483.1:n.-222_-221insA
NM_001135662.1:c.-131+10_-131+11insA NP_001129134.1:n.-131+10_-131+11insA
NM_001135663.1:c.-408_-407insA NP_001129135.1:n.-408_-407insA
NM_001135664.1:c.-184_-183insA NP_001129136.1:n.-184_-183insA
NM_003929.2:c.-222_-221insA NP_003920.1:n.-222_-221insA
XM_005245569.1:c.-136+10_-136+11insA XP_005245626.1:n.-136+10_-136+11insA
XM_005245570.1:c.-227_-226insA XP_005245627.1:n.-227_-226insA
XM_005245571.1:c.-131+38_-131+39insA XP_005245628.1:n.-131+38_-131+39insA
XM_006711605.2:c.-93+10_-93+11insA XP_006711668.1:n.-93+10_-93+11insA
XM_006711606.1:c.-93+38_-93+39insA XP_006711669.1:n.-93+38_-93+39insA
XM_006711605.3:c.-93+10_-93+11insA XP_006711668.1:n.-93+10_-93+11insA
XM_006711606.3:c.-93+38_-93+39insA XP_006711669.1:n.-93+38_-93+39insA
XM_017002748.1:c.-222_-221insA XP_016858237.1:n.-222_-221insA
XM_017002749.1:c.-227_-226insA XP_016858238.1:n.-227_-226insA
XM_017002750.1:c.-131+10_-131+11insA XP_016858239.1:n.-131+10_-131+11insA
NM_003929.3:c.-222_-221insA MANE Select NP_003920.1:n.-222_-221insA
NM_001135662.2:c.-131+10_-131+11insA NP_001129134.1:n.-131+10_-131+11insA
NM_001135663.2:c.-408_-407insA NP_001129135.1:n.-408_-407insA
NM_001135664.2:c.-184_-183insA NP_001129136.1:n.-184_-183insA