Canonical Allele Identifier: CA2650150834

Gene: RAB29

Linked Data

• gnomAD v4: 1-205775356-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775360del , CM000663.2:g.205775360del	GRCh38
NC_000001.10:g.205744488del , CM000663.1:g.205744488del	GRCh37
NC_000001.9:g.204011111del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-215del MANE Select	ENSP00000356107.3:n.-215del
ENST00000235932.8:c.-131+17del	ENSP00000235932.4:n.-131+17del
ENST00000367139.7:c.-215del	ENSP00000356107.3:n.-215del
ENST00000414729.1:c.-401del	ENSP00000402910.1:n.-401del
ENST00000437324.6:c.-177del	ENSP00000416613.2:n.-177del
ENST00000468887.1:n.84del
ENST00000528078.1:c.-215del	ENSP00000431483.1:n.-215del
NM_001135662.1:c.-131+17del	NP_001129134.1:n.-131+17del
NM_001135663.1:c.-401del	NP_001129135.1:n.-401del
NM_001135664.1:c.-177del	NP_001129136.1:n.-177del
NM_003929.2:c.-215del	NP_003920.1:n.-215del
XM_005245569.1:c.-136+17del	XP_005245626.1:n.-136+17del
XM_005245570.1:c.-220del	XP_005245627.1:n.-220del
XM_005245571.1:c.-131+45del	XP_005245628.1:n.-131+45del
XM_006711605.2:c.-93+17del	XP_006711668.1:n.-93+17del
XM_006711606.1:c.-93+45del	XP_006711669.1:n.-93+45del
XM_006711605.3:c.-93+17del	XP_006711668.1:n.-93+17del
XM_006711606.3:c.-93+45del	XP_006711669.1:n.-93+45del
XM_017002748.1:c.-215del	XP_016858237.1:n.-215del
XM_017002749.1:c.-220del	XP_016858238.1:n.-220del
XM_017002750.1:c.-131+17del	XP_016858239.1:n.-131+17del
NM_003929.3:c.-215del MANE Select	NP_003920.1:n.-215del
NM_001135662.2:c.-131+17del	NP_001129134.1:n.-131+17del
NM_001135663.2:c.-401del	NP_001129135.1:n.-401del
NM_001135664.2:c.-177del	NP_001129136.1:n.-177del