Canonical Allele Identifier: CA2650149145

Gene: RAB29

Linked Data

• gnomAD v4: 1-205774792-T-TCCGCCAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205774794_205774795insGCCAGCCC , CM000663.2:g.205774794_205774795insGCCAGCCC	GRCh38
NC_000001.10:g.205743922_205743923insGCCAGCCC , CM000663.1:g.205743922_205743923insGCCAGCCC	GRCh37
NC_000001.9:g.204010545_204010546insGCCAGCCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.124+40_124+41insGCTGGCGG MANE Select	ENSP00000356107.3:n.124+40_124+41insGCTGGCGG
ENST00000235932.8:c.124+40_124+41insGCTGGCGG	ENSP00000235932.4:n.124+40_124+41insGCTGGCGG
ENST00000367139.7:c.124+40_124+41insGCTGGCGG	ENSP00000356107.3:n.124+40_124+41insGCTGGCGG
ENST00000414729.1:c.124+40_124+41insGCTGGCGG	ENSP00000402910.1:n.124+40_124+41insGCTGGCGG
ENST00000437324.6:c.-93+480_-93+481insGCTGGCGG	ENSP00000416613.2:n.-93+480_-93+481insGCTGGCGG
ENST00000446390.6:c.124+40_124+41insGCTGGCGG	ENSP00000389899.2:n.124+40_124+41insGCTGGCGG
ENST00000468887.1:n.168+480_168+481insGCTGGCGG
ENST00000492534.1:n.319+40_319+41insGCTGGCGG
ENST00000528078.1:c.124+40_124+41insGCTGGCGG	ENSP00000431483.1:n.124+40_124+41insGCTGGCGG
ENST00000533111.1:n.81+336_81+337insGCTGGCGG
NM_001135662.1:c.124+40_124+41insGCTGGCGG	NP_001129134.1:n.124+40_124+41insGCTGGCGG
NM_001135663.1:c.124+40_124+41insGCTGGCGG	NP_001129135.1:n.124+40_124+41insGCTGGCGG
NM_001135664.1:c.-93+480_-93+481insGCTGGCGG	NP_001129136.1:n.-93+480_-93+481insGCTGGCGG
NM_003929.2:c.124+40_124+41insGCTGGCGG	NP_003920.1:n.124+40_124+41insGCTGGCGG
XM_005245569.1:c.124+40_124+41insGCTGGCGG	XP_005245626.1:n.124+40_124+41insGCTGGCGG
XM_005245570.1:c.124+40_124+41insGCTGGCGG	XP_005245627.1:n.124+40_124+41insGCTGGCGG
XM_005245571.1:c.124+40_124+41insGCTGGCGG	XP_005245628.1:n.124+40_124+41insGCTGGCGG
XM_006711605.2:c.-93+581_-93+582insGCTGGCGG	XP_006711668.1:n.-93+581_-93+582insGCTGGCGG
XM_006711606.1:c.-93+609_-93+610insGCTGGCGG	XP_006711669.1:n.-93+609_-93+610insGCTGGCGG
XM_006711605.3:c.-93+581_-93+582insGCTGGCGG	XP_006711668.1:n.-93+581_-93+582insGCTGGCGG
XM_006711606.3:c.-93+609_-93+610insGCTGGCGG	XP_006711669.1:n.-93+609_-93+610insGCTGGCGG
XM_017002748.1:c.124+40_124+41insGCTGGCGG	XP_016858237.1:n.124+40_124+41insGCTGGCGG
XM_017002749.1:c.124+40_124+41insGCTGGCGG	XP_016858238.1:n.124+40_124+41insGCTGGCGG
XM_017002750.1:c.124+40_124+41insGCTGGCGG	XP_016858239.1:n.124+40_124+41insGCTGGCGG
NM_003929.3:c.124+40_124+41insGCTGGCGG MANE Select	NP_003920.1:n.124+40_124+41insGCTGGCGG
NM_001135662.2:c.124+40_124+41insGCTGGCGG	NP_001129134.1:n.124+40_124+41insGCTGGCGG
NM_001135663.2:c.124+40_124+41insGCTGGCGG	NP_001129135.1:n.124+40_124+41insGCTGGCGG
NM_001135664.2:c.-93+480_-93+481insGCTGGCGG	NP_001129136.1:n.-93+480_-93+481insGCTGGCGG