Canonical Allele Identifier: CA2650150818

Gene: RAB29

Linked Data

• gnomAD v4: 1-205775346-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775346A>C , CM000663.2:g.205775346A>C	GRCh38
NC_000001.10:g.205744474A>C , CM000663.1:g.205744474A>C	GRCh37
NC_000001.9:g.204011097A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-204T>G MANE Select	ENSP00000356107.3:n.-204T>G
ENST00000235932.8:c.-131+28T>G	ENSP00000235932.4:n.-131+28T>G
ENST00000367139.7:c.-204T>G	ENSP00000356107.3:n.-204T>G
ENST00000414729.1:c.-390T>G	ENSP00000402910.1:n.-390T>G
ENST00000437324.6:c.-166T>G	ENSP00000416613.2:n.-166T>G
ENST00000468887.1:n.95T>G
ENST00000528078.1:c.-204T>G	ENSP00000431483.1:n.-204T>G
NM_001135662.1:c.-131+28T>G	NP_001129134.1:n.-131+28T>G
NM_001135663.1:c.-390T>G	NP_001129135.1:n.-390T>G
NM_001135664.1:c.-166T>G	NP_001129136.1:n.-166T>G
NM_003929.2:c.-204T>G	NP_003920.1:n.-204T>G
XM_005245569.1:c.-136+28T>G	XP_005245626.1:n.-136+28T>G
XM_005245570.1:c.-209T>G	XP_005245627.1:n.-209T>G
XM_005245571.1:c.-131+56T>G	XP_005245628.1:n.-131+56T>G
XM_006711605.2:c.-93+28T>G	XP_006711668.1:n.-93+28T>G
XM_006711606.1:c.-93+56T>G	XP_006711669.1:n.-93+56T>G
XM_006711605.3:c.-93+28T>G	XP_006711668.1:n.-93+28T>G
XM_006711606.3:c.-93+56T>G	XP_006711669.1:n.-93+56T>G
XM_017002748.1:c.-204T>G	XP_016858237.1:n.-204T>G
XM_017002749.1:c.-209T>G	XP_016858238.1:n.-209T>G
XM_017002750.1:c.-131+28T>G	XP_016858239.1:n.-131+28T>G
NM_003929.3:c.-204T>G MANE Select	NP_003920.1:n.-204T>G
NM_001135662.2:c.-131+28T>G	NP_001129134.1:n.-131+28T>G
NM_001135663.2:c.-390T>G	NP_001129135.1:n.-390T>G
NM_001135664.2:c.-166T>G	NP_001129136.1:n.-166T>G