Canonical Allele Identifier: CA2650150813

Gene: RAB29

Linked Data

• gnomAD v4: 1-205775338-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775340del , CM000663.2:g.205775340del	GRCh38
NC_000001.10:g.205744468del , CM000663.1:g.205744468del	GRCh37
NC_000001.9:g.204011091del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-197del MANE Select	ENSP00000356107.3:n.-197del
ENST00000235932.8:c.-131+35del	ENSP00000235932.4:n.-131+35del
ENST00000367139.7:c.-197del	ENSP00000356107.3:n.-197del
ENST00000414729.1:c.-383del	ENSP00000402910.1:n.-383del
ENST00000437324.6:c.-159del	ENSP00000416613.2:n.-159del
ENST00000468887.1:n.102del
ENST00000528078.1:c.-197del	ENSP00000431483.1:n.-197del
NM_001135662.1:c.-131+35del	NP_001129134.1:n.-131+35del
NM_001135663.1:c.-383del	NP_001129135.1:n.-383del
NM_001135664.1:c.-159del	NP_001129136.1:n.-159del
NM_003929.2:c.-197del	NP_003920.1:n.-197del
XM_005245569.1:c.-136+35del	XP_005245626.1:n.-136+35del
XM_005245570.1:c.-202del	XP_005245627.1:n.-202del
XM_005245571.1:c.-131+63del	XP_005245628.1:n.-131+63del
XM_006711605.2:c.-93+35del	XP_006711668.1:n.-93+35del
XM_006711606.1:c.-93+63del	XP_006711669.1:n.-93+63del
XM_006711605.3:c.-93+35del	XP_006711668.1:n.-93+35del
XM_006711606.3:c.-93+63del	XP_006711669.1:n.-93+63del
XM_017002748.1:c.-197del	XP_016858237.1:n.-197del
XM_017002749.1:c.-202del	XP_016858238.1:n.-202del
XM_017002750.1:c.-131+35del	XP_016858239.1:n.-131+35del
NM_003929.3:c.-197del MANE Select	NP_003920.1:n.-197del
NM_001135662.2:c.-131+35del	NP_001129134.1:n.-131+35del
NM_001135663.2:c.-383del	NP_001129135.1:n.-383del
NM_001135664.2:c.-159del	NP_001129136.1:n.-159del