Canonical Allele Identifier: CA2581733262

Gene: RAB29

Linked Data

• dbSNP Id: rs1572931
• gnomAD v4: 1-205775090-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775090C>G , CM000663.2:g.205775090C>G	GRCh38
NC_000001.10:g.205744218C>G , CM000663.1:g.205744218C>G	GRCh37
NC_000001.9:g.204010841C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000367139.8:c.-130-4G>C MANE Select	ENSP00000356107.3:n.-130-4G>C
ENST00000235932.8:c.-130-4G>C	ENSP00000235932.4:n.-130-4G>C
ENST00000367139.7:c.-130-4G>C	ENSP00000356107.3:n.-130-4G>C
ENST00000414729.1:c.-134G>C	ENSP00000402910.1:n.-134G>C
ENST00000437324.6:c.-93+183G>C	ENSP00000416613.2:n.-93+183G>C
ENST00000446390.6:c.-134G>C	ENSP00000389899.2:n.-134G>C
ENST00000468887.1:n.168+183G>C
ENST00000492534.1:n.62G>C
ENST00000528078.1:c.-130-4G>C	ENSP00000431483.1:n.-130-4G>C
ENST00000533111.1:n.81+39G>C
NM_001135662.1:c.-130-4G>C	NP_001129134.1:n.-130-4G>C
NM_001135663.1:c.-134G>C	NP_001129135.1:n.-134G>C
NM_001135664.1:c.-93+183G>C	NP_001129136.1:n.-93+183G>C
NM_003929.2:c.-130-4G>C	NP_003920.1:n.-130-4G>C
XM_005245569.1:c.-134G>C	XP_005245626.1:n.-134G>C
XM_005245570.1:c.-134G>C	XP_005245627.1:n.-134G>C
XM_005245571.1:c.-130-4G>C	XP_005245628.1:n.-130-4G>C
XM_006711605.2:c.-93+284G>C	XP_006711668.1:n.-93+284G>C
XM_006711606.1:c.-93+312G>C	XP_006711669.1:n.-93+312G>C
XM_006711605.3:c.-93+284G>C	XP_006711668.1:n.-93+284G>C
XM_006711606.3:c.-93+312G>C	XP_006711669.1:n.-93+312G>C
XM_017002748.1:c.-130-4G>C	XP_016858237.1:n.-130-4G>C
XM_017002749.1:c.-134G>C	XP_016858238.1:n.-134G>C
XM_017002750.1:c.-130-4G>C	XP_016858239.1:n.-130-4G>C
NM_003929.3:c.-130-4G>C MANE Select	NP_003920.1:n.-130-4G>C
NM_001135662.2:c.-130-4G>C	NP_001129134.1:n.-130-4G>C
NM_001135663.2:c.-134G>C	NP_001129135.1:n.-134G>C
NM_001135664.2:c.-93+183G>C	NP_001129136.1:n.-93+183G>C