Canonical Allele Identifier: CA2650150773

Gene: RAB29

Linked Data

• gnomAD v4: 1-205775324-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775326del , CM000663.2:g.205775326del	GRCh38
NC_000001.10:g.205744454del , CM000663.1:g.205744454del	GRCh37
NC_000001.9:g.204011077del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-183del MANE Select	ENSP00000356107.3:n.-183del
ENST00000235932.8:c.-131+49del	ENSP00000235932.4:n.-131+49del
ENST00000367139.7:c.-183del	ENSP00000356107.3:n.-183del
ENST00000414729.1:c.-369del	ENSP00000402910.1:n.-369del
ENST00000437324.6:c.-145del	ENSP00000416613.2:n.-145del
ENST00000468887.1:n.116del
ENST00000528078.1:c.-183del	ENSP00000431483.1:n.-183del
NM_001135662.1:c.-131+49del	NP_001129134.1:n.-131+49del
NM_001135663.1:c.-369del	NP_001129135.1:n.-369del
NM_001135664.1:c.-145del	NP_001129136.1:n.-145del
NM_003929.2:c.-183del	NP_003920.1:n.-183del
XM_005245569.1:c.-136+49del	XP_005245626.1:n.-136+49del
XM_005245570.1:c.-188del	XP_005245627.1:n.-188del
XM_005245571.1:c.-131+77del	XP_005245628.1:n.-131+77del
XM_006711605.2:c.-93+49del	XP_006711668.1:n.-93+49del
XM_006711606.1:c.-93+77del	XP_006711669.1:n.-93+77del
XM_006711605.3:c.-93+49del	XP_006711668.1:n.-93+49del
XM_006711606.3:c.-93+77del	XP_006711669.1:n.-93+77del
XM_017002748.1:c.-183del	XP_016858237.1:n.-183del
XM_017002749.1:c.-188del	XP_016858238.1:n.-188del
XM_017002750.1:c.-131+49del	XP_016858239.1:n.-131+49del
NM_003929.3:c.-183del MANE Select	NP_003920.1:n.-183del
NM_001135662.2:c.-131+49del	NP_001129134.1:n.-131+49del
NM_001135663.2:c.-369del	NP_001129135.1:n.-369del
NM_001135664.2:c.-145del	NP_001129136.1:n.-145del