Canonical Allele Identifier: CA2650149175

Gene: RAB29

Linked Data

• gnomAD v4: 1-205774793-C-CCGGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205774794_205774795insGGCAC , CM000663.2:g.205774794_205774795insGGCAC	GRCh38
NC_000001.10:g.205743922_205743923insGGCAC , CM000663.1:g.205743922_205743923insGGCAC	GRCh37
NC_000001.9:g.204010545_204010546insGGCAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.124+39_124+40insTGCCG MANE Select	ENSP00000356107.3:n.124+39_124+40insTGCCG
ENST00000235932.8:c.124+39_124+40insTGCCG	ENSP00000235932.4:n.124+39_124+40insTGCCG
ENST00000367139.7:c.124+39_124+40insTGCCG	ENSP00000356107.3:n.124+39_124+40insTGCCG
ENST00000414729.1:c.124+39_124+40insTGCCG	ENSP00000402910.1:n.124+39_124+40insTGCCG
ENST00000437324.6:c.-93+479_-93+480insTGCCG	ENSP00000416613.2:n.-93+479_-93+480insTGCCG
ENST00000446390.6:c.124+39_124+40insTGCCG	ENSP00000389899.2:n.124+39_124+40insTGCCG
ENST00000468887.1:n.168+479_168+480insTGCCG
ENST00000492534.1:n.319+39_319+40insTGCCG
ENST00000528078.1:c.124+39_124+40insTGCCG	ENSP00000431483.1:n.124+39_124+40insTGCCG
ENST00000533111.1:n.81+335_81+336insTGCCG
NM_001135662.1:c.124+39_124+40insTGCCG	NP_001129134.1:n.124+39_124+40insTGCCG
NM_001135663.1:c.124+39_124+40insTGCCG	NP_001129135.1:n.124+39_124+40insTGCCG
NM_001135664.1:c.-93+479_-93+480insTGCCG	NP_001129136.1:n.-93+479_-93+480insTGCCG
NM_003929.2:c.124+39_124+40insTGCCG	NP_003920.1:n.124+39_124+40insTGCCG
XM_005245569.1:c.124+39_124+40insTGCCG	XP_005245626.1:n.124+39_124+40insTGCCG
XM_005245570.1:c.124+39_124+40insTGCCG	XP_005245627.1:n.124+39_124+40insTGCCG
XM_005245571.1:c.124+39_124+40insTGCCG	XP_005245628.1:n.124+39_124+40insTGCCG
XM_006711605.2:c.-93+580_-93+581insTGCCG	XP_006711668.1:n.-93+580_-93+581insTGCCG
XM_006711606.1:c.-93+608_-93+609insTGCCG	XP_006711669.1:n.-93+608_-93+609insTGCCG
XM_006711605.3:c.-93+580_-93+581insTGCCG	XP_006711668.1:n.-93+580_-93+581insTGCCG
XM_006711606.3:c.-93+608_-93+609insTGCCG	XP_006711669.1:n.-93+608_-93+609insTGCCG
XM_017002748.1:c.124+39_124+40insTGCCG	XP_016858237.1:n.124+39_124+40insTGCCG
XM_017002749.1:c.124+39_124+40insTGCCG	XP_016858238.1:n.124+39_124+40insTGCCG
XM_017002750.1:c.124+39_124+40insTGCCG	XP_016858239.1:n.124+39_124+40insTGCCG
NM_003929.3:c.124+39_124+40insTGCCG MANE Select	NP_003920.1:n.124+39_124+40insTGCCG
NM_001135662.2:c.124+39_124+40insTGCCG	NP_001129134.1:n.124+39_124+40insTGCCG
NM_001135663.2:c.124+39_124+40insTGCCG	NP_001129135.1:n.124+39_124+40insTGCCG
NM_001135664.2:c.-93+479_-93+480insTGCCG	NP_001129136.1:n.-93+479_-93+480insTGCCG