Canonical Allele Identifier: CA1011510143
Gene: RAB29 HGNC NCBI

Linked Data

dbSNP Id: rs1655268855

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205775283_205775304dup , CM000663.2:g.205775283_205775304dup GRCh38
NC_000001.10:g.205744411_205744432dup , CM000663.1:g.205744411_205744432dup GRCh37
NC_000001.9:g.204011034_204011055dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367139.8:c.-162_-141dup MANE Select ENSP00000356107.3:n.-162_-141dup
ENST00000235932.8:c.-131+70_-131+91dup ENSP00000235932.4:n.-131+70_-131+91dup
ENST00000367139.7:c.-162_-141dup ENSP00000356107.3:n.-162_-141dup
ENST00000414729.1:c.-348_-327dup ENSP00000402910.1:n.-348_-327dup
ENST00000437324.6:c.-124_-103dup ENSP00000416613.2:n.-124_-103dup
ENST00000468887.1:n.137_158dup
ENST00000528078.1:c.-162_-141dup ENSP00000431483.1:n.-162_-141dup
NM_001135662.1:c.-131+70_-131+91dup NP_001129134.1:n.-131+70_-131+91dup
NM_001135663.1:c.-348_-327dup NP_001129135.1:n.-348_-327dup
NM_001135664.1:c.-124_-103dup NP_001129136.1:n.-124_-103dup
NM_003929.2:c.-162_-141dup NP_003920.1:n.-162_-141dup
XM_005245569.1:c.-136+70_-136+91dup XP_005245626.1:n.-136+70_-136+91dup
XM_005245570.1:c.-167_-146dup XP_005245627.1:n.-167_-146dup
XM_005245571.1:c.-131+98_-131+119dup XP_005245628.1:n.-131+98_-131+119dup
XM_006711605.2:c.-93+70_-93+91dup XP_006711668.1:n.-93+70_-93+91dup
XM_006711606.1:c.-93+98_-93+119dup XP_006711669.1:n.-93+98_-93+119dup
XM_006711605.3:c.-93+70_-93+91dup XP_006711668.1:n.-93+70_-93+91dup
XM_006711606.3:c.-93+98_-93+119dup XP_006711669.1:n.-93+98_-93+119dup
XM_017002748.1:c.-162_-141dup XP_016858237.1:n.-162_-141dup
XM_017002749.1:c.-167_-146dup XP_016858238.1:n.-167_-146dup
XM_017002750.1:c.-131+70_-131+91dup XP_016858239.1:n.-131+70_-131+91dup
NM_003929.3:c.-162_-141dup MANE Select NP_003920.1:n.-162_-141dup
NM_001135662.2:c.-131+70_-131+91dup NP_001129134.1:n.-131+70_-131+91dup
NM_001135663.2:c.-348_-327dup NP_001129135.1:n.-348_-327dup
NM_001135664.2:c.-124_-103dup NP_001129136.1:n.-124_-103dup