Canonical Allele Identifier: CA2650150709

Gene: RAB29

Linked Data

• gnomAD v4: 1-205775280-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775285dup , CM000663.2:g.205775285dup	GRCh38
NC_000001.10:g.205744413dup , CM000663.1:g.205744413dup	GRCh37
NC_000001.9:g.204011036dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-139dup MANE Select	ENSP00000356107.3:n.-139dup
ENST00000235932.8:c.-131+93dup	ENSP00000235932.4:n.-131+93dup
ENST00000367139.7:c.-139dup	ENSP00000356107.3:n.-139dup
ENST00000414729.1:c.-325dup	ENSP00000402910.1:n.-325dup
ENST00000437324.6:c.-101dup	ENSP00000416613.2:n.-101dup
ENST00000468887.1:n.160dup
ENST00000528078.1:c.-139dup	ENSP00000431483.1:n.-139dup
NM_001135662.1:c.-131+93dup	NP_001129134.1:n.-131+93dup
NM_001135663.1:c.-325dup	NP_001129135.1:n.-325dup
NM_001135664.1:c.-101dup	NP_001129136.1:n.-101dup
NM_003929.2:c.-139dup	NP_003920.1:n.-139dup
XM_005245569.1:c.-136+93dup	XP_005245626.1:n.-136+93dup
XM_005245570.1:c.-144dup	XP_005245627.1:n.-144dup
XM_005245571.1:c.-131+121dup	XP_005245628.1:n.-131+121dup
XM_006711605.2:c.-93+93dup	XP_006711668.1:n.-93+93dup
XM_006711606.1:c.-93+121dup	XP_006711669.1:n.-93+121dup
XM_006711605.3:c.-93+93dup	XP_006711668.1:n.-93+93dup
XM_006711606.3:c.-93+121dup	XP_006711669.1:n.-93+121dup
XM_017002748.1:c.-139dup	XP_016858237.1:n.-139dup
XM_017002749.1:c.-144dup	XP_016858238.1:n.-144dup
XM_017002750.1:c.-131+93dup	XP_016858239.1:n.-131+93dup
NM_003929.3:c.-139dup MANE Select	NP_003920.1:n.-139dup
NM_001135662.2:c.-131+93dup	NP_001129134.1:n.-131+93dup
NM_001135663.2:c.-325dup	NP_001129135.1:n.-325dup
NM_001135664.2:c.-101dup	NP_001129136.1:n.-101dup