Canonical Allele Identifier: CA1011510146

Gene: RAB29

Linked Data

• dbSNP Id: rs1655269335
• gnomAD v3: 1-205775292-C-T
• gnomAD v4: 1-205775292-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775292C>T , CM000663.2:g.205775292C>T	GRCh38
NC_000001.10:g.205744420C>T , CM000663.1:g.205744420C>T	GRCh37
NC_000001.9:g.204011043C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-150G>A MANE Select	ENSP00000356107.3:n.-150G>A
ENST00000235932.8:c.-131+82G>A	ENSP00000235932.4:n.-131+82G>A
ENST00000367139.7:c.-150G>A	ENSP00000356107.3:n.-150G>A
ENST00000414729.1:c.-336G>A	ENSP00000402910.1:n.-336G>A
ENST00000437324.6:c.-112G>A	ENSP00000416613.2:n.-112G>A
ENST00000468887.1:n.149G>A
ENST00000528078.1:c.-150G>A	ENSP00000431483.1:n.-150G>A
NM_001135662.1:c.-131+82G>A	NP_001129134.1:n.-131+82G>A
NM_001135663.1:c.-336G>A	NP_001129135.1:n.-336G>A
NM_001135664.1:c.-112G>A	NP_001129136.1:n.-112G>A
NM_003929.2:c.-150G>A	NP_003920.1:n.-150G>A
XM_005245569.1:c.-136+82G>A	XP_005245626.1:n.-136+82G>A
XM_005245570.1:c.-155G>A	XP_005245627.1:n.-155G>A
XM_005245571.1:c.-131+110G>A	XP_005245628.1:n.-131+110G>A
XM_006711605.2:c.-93+82G>A	XP_006711668.1:n.-93+82G>A
XM_006711606.1:c.-93+110G>A	XP_006711669.1:n.-93+110G>A
XM_006711605.3:c.-93+82G>A	XP_006711668.1:n.-93+82G>A
XM_006711606.3:c.-93+110G>A	XP_006711669.1:n.-93+110G>A
XM_017002748.1:c.-150G>A	XP_016858237.1:n.-150G>A
XM_017002749.1:c.-155G>A	XP_016858238.1:n.-155G>A
XM_017002750.1:c.-131+82G>A	XP_016858239.1:n.-131+82G>A
NM_003929.3:c.-150G>A MANE Select	NP_003920.1:n.-150G>A
NM_001135662.2:c.-131+82G>A	NP_001129134.1:n.-131+82G>A
NM_001135663.2:c.-336G>A	NP_001129135.1:n.-336G>A
NM_001135664.2:c.-112G>A	NP_001129136.1:n.-112G>A