Canonical Allele Identifier: CA2650150771

Gene: RAB29

Linked Data

• gnomAD v4: 1-205775323-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775323C>A , CM000663.2:g.205775323C>A	GRCh38
NC_000001.10:g.205744451C>A , CM000663.1:g.205744451C>A	GRCh37
NC_000001.9:g.204011074C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-181G>T MANE Select	ENSP00000356107.3:n.-181G>T
ENST00000235932.8:c.-131+51G>T	ENSP00000235932.4:n.-131+51G>T
ENST00000367139.7:c.-181G>T	ENSP00000356107.3:n.-181G>T
ENST00000414729.1:c.-367G>T	ENSP00000402910.1:n.-367G>T
ENST00000437324.6:c.-143G>T	ENSP00000416613.2:n.-143G>T
ENST00000468887.1:n.118G>T
ENST00000528078.1:c.-181G>T	ENSP00000431483.1:n.-181G>T
NM_001135662.1:c.-131+51G>T	NP_001129134.1:n.-131+51G>T
NM_001135663.1:c.-367G>T	NP_001129135.1:n.-367G>T
NM_001135664.1:c.-143G>T	NP_001129136.1:n.-143G>T
NM_003929.2:c.-181G>T	NP_003920.1:n.-181G>T
XM_005245569.1:c.-136+51G>T	XP_005245626.1:n.-136+51G>T
XM_005245570.1:c.-186G>T	XP_005245627.1:n.-186G>T
XM_005245571.1:c.-131+79G>T	XP_005245628.1:n.-131+79G>T
XM_006711605.2:c.-93+51G>T	XP_006711668.1:n.-93+51G>T
XM_006711606.1:c.-93+79G>T	XP_006711669.1:n.-93+79G>T
XM_006711605.3:c.-93+51G>T	XP_006711668.1:n.-93+51G>T
XM_006711606.3:c.-93+79G>T	XP_006711669.1:n.-93+79G>T
XM_017002748.1:c.-181G>T	XP_016858237.1:n.-181G>T
XM_017002749.1:c.-186G>T	XP_016858238.1:n.-186G>T
XM_017002750.1:c.-131+51G>T	XP_016858239.1:n.-131+51G>T
NM_003929.3:c.-181G>T MANE Select	NP_003920.1:n.-181G>T
NM_001135662.2:c.-131+51G>T	NP_001129134.1:n.-131+51G>T
NM_001135663.2:c.-367G>T	NP_001129135.1:n.-367G>T
NM_001135664.2:c.-143G>T	NP_001129136.1:n.-143G>T