Canonical Allele Identifier: CA2650150558

Gene: RAB29

Linked Data

• gnomAD v4: 1-205775226-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775226G>T , CM000663.2:g.205775226G>T	GRCh38
NC_000001.10:g.205744354G>T , CM000663.1:g.205744354G>T	GRCh37
NC_000001.9:g.204010977G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-131+47C>A MANE Select	ENSP00000356107.3:n.-131+47C>A
ENST00000235932.8:c.-130-140C>A	ENSP00000235932.4:n.-130-140C>A
ENST00000367139.7:c.-131+47C>A	ENSP00000356107.3:n.-131+47C>A
ENST00000414729.1:c.-270C>A	ENSP00000402910.1:n.-270C>A
ENST00000437324.6:c.-93+47C>A	ENSP00000416613.2:n.-93+47C>A
ENST00000446390.6:c.-270C>A	ENSP00000389899.2:n.-270C>A
ENST00000468887.1:n.168+47C>A
ENST00000528078.1:c.-131+47C>A	ENSP00000431483.1:n.-131+47C>A
NM_001135662.1:c.-130-140C>A	NP_001129134.1:n.-130-140C>A
NM_001135663.1:c.-270C>A	NP_001129135.1:n.-270C>A
NM_001135664.1:c.-93+47C>A	NP_001129136.1:n.-93+47C>A
NM_003929.2:c.-131+47C>A	NP_003920.1:n.-131+47C>A
XM_005245569.1:c.-135-135C>A	XP_005245626.1:n.-135-135C>A
XM_005245570.1:c.-136+47C>A	XP_005245627.1:n.-136+47C>A
XM_005245571.1:c.-130-140C>A	XP_005245628.1:n.-130-140C>A
XM_006711605.2:c.-93+148C>A	XP_006711668.1:n.-93+148C>A
XM_006711606.1:c.-93+176C>A	XP_006711669.1:n.-93+176C>A
XM_006711605.3:c.-93+148C>A	XP_006711668.1:n.-93+148C>A
XM_006711606.3:c.-93+176C>A	XP_006711669.1:n.-93+176C>A
XM_017002748.1:c.-131+47C>A	XP_016858237.1:n.-131+47C>A
XM_017002749.1:c.-136+47C>A	XP_016858238.1:n.-136+47C>A
XM_017002750.1:c.-130-140C>A	XP_016858239.1:n.-130-140C>A
NM_003929.3:c.-131+47C>A MANE Select	NP_003920.1:n.-131+47C>A
NM_001135662.2:c.-130-140C>A	NP_001129134.1:n.-130-140C>A
NM_001135663.2:c.-270C>A	NP_001129135.1:n.-270C>A
NM_001135664.2:c.-93+47C>A	NP_001129136.1:n.-93+47C>A