Canonical Allele Identifier: CA2650150784

Gene: RAB29

Linked Data

• gnomAD v4: 1-205775328-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775328C>T , CM000663.2:g.205775328C>T	GRCh38
NC_000001.10:g.205744456C>T , CM000663.1:g.205744456C>T	GRCh37
NC_000001.9:g.204011079C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-186G>A MANE Select	ENSP00000356107.3:n.-186G>A
ENST00000235932.8:c.-131+46G>A	ENSP00000235932.4:n.-131+46G>A
ENST00000367139.7:c.-186G>A	ENSP00000356107.3:n.-186G>A
ENST00000414729.1:c.-372G>A	ENSP00000402910.1:n.-372G>A
ENST00000437324.6:c.-148G>A	ENSP00000416613.2:n.-148G>A
ENST00000468887.1:n.113G>A
ENST00000528078.1:c.-186G>A	ENSP00000431483.1:n.-186G>A
NM_001135662.1:c.-131+46G>A	NP_001129134.1:n.-131+46G>A
NM_001135663.1:c.-372G>A	NP_001129135.1:n.-372G>A
NM_001135664.1:c.-148G>A	NP_001129136.1:n.-148G>A
NM_003929.2:c.-186G>A	NP_003920.1:n.-186G>A
XM_005245569.1:c.-136+46G>A	XP_005245626.1:n.-136+46G>A
XM_005245570.1:c.-191G>A	XP_005245627.1:n.-191G>A
XM_005245571.1:c.-131+74G>A	XP_005245628.1:n.-131+74G>A
XM_006711605.2:c.-93+46G>A	XP_006711668.1:n.-93+46G>A
XM_006711606.1:c.-93+74G>A	XP_006711669.1:n.-93+74G>A
XM_006711605.3:c.-93+46G>A	XP_006711668.1:n.-93+46G>A
XM_006711606.3:c.-93+74G>A	XP_006711669.1:n.-93+74G>A
XM_017002748.1:c.-186G>A	XP_016858237.1:n.-186G>A
XM_017002749.1:c.-191G>A	XP_016858238.1:n.-191G>A
XM_017002750.1:c.-131+46G>A	XP_016858239.1:n.-131+46G>A
NM_003929.3:c.-186G>A MANE Select	NP_003920.1:n.-186G>A
NM_001135662.2:c.-131+46G>A	NP_001129134.1:n.-131+46G>A
NM_001135663.2:c.-372G>A	NP_001129135.1:n.-372G>A
NM_001135664.2:c.-148G>A	NP_001129136.1:n.-148G>A