Canonical Allele Identifier: CA1011509705

Gene: RAB29

Linked Data

• gnomAD v3: 1-205774795-T-TCCCCCCCCCCCCC
• gnomAD v4: 1-205774795-T-TCCCCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205774797_205774798insCCCCCCCCCCCCC , CM000663.2:g.205774797_205774798insCCCCCCCCCCCCC	GRCh38
NC_000001.10:g.205743925_205743926insCCCCCCCCCCCCC , CM000663.1:g.205743925_205743926insCCCCCCCCCCCCC	GRCh37
NC_000001.9:g.204010548_204010549insCCCCCCCCCCCCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.124+37_124+38insGGGGGGGGGGGGG MANE Select	ENSP00000356107.3:n.124+37_124+38insGGGGGGGGGGGGG
ENST00000235932.8:c.124+37_124+38insGGGGGGGGGGGGG	ENSP00000235932.4:n.124+37_124+38insGGGGGGGGGGGGG
ENST00000367139.7:c.124+37_124+38insGGGGGGGGGGGGG	ENSP00000356107.3:n.124+37_124+38insGGGGGGGGGGGGG
ENST00000414729.1:c.124+37_124+38insGGGGGGGGGGGGG	ENSP00000402910.1:n.124+37_124+38insGGGGGGGGGGGGG
ENST00000437324.6:c.-93+477_-93+478insGGGGGGGGGGGGG	ENSP00000416613.2:n.-93+477_-93+478insGGGGGGGGGGGGG
ENST00000446390.6:c.124+37_124+38insGGGGGGGGGGGGG	ENSP00000389899.2:n.124+37_124+38insGGGGGGGGGGGGG
ENST00000468887.1:n.168+477_168+478insGGGGGGGGGGGGG
ENST00000492534.1:n.319+37_319+38insGGGGGGGGGGGGG
ENST00000528078.1:c.124+37_124+38insGGGGGGGGGGGGG	ENSP00000431483.1:n.124+37_124+38insGGGGGGGGGGGGG
ENST00000533111.1:n.81+333_81+334insGGGGGGGGGGGGG
NM_001135662.1:c.124+37_124+38insGGGGGGGGGGGGG	NP_001129134.1:n.124+37_124+38insGGGGGGGGGGGGG
NM_001135663.1:c.124+37_124+38insGGGGGGGGGGGGG	NP_001129135.1:n.124+37_124+38insGGGGGGGGGGGGG
NM_001135664.1:c.-93+477_-93+478insGGGGGGGGGGGGG	NP_001129136.1:n.-93+477_-93+478insGGGGGGGGGGGGG
NM_003929.2:c.124+37_124+38insGGGGGGGGGGGGG	NP_003920.1:n.124+37_124+38insGGGGGGGGGGGGG
XM_005245569.1:c.124+37_124+38insGGGGGGGGGGGGG	XP_005245626.1:n.124+37_124+38insGGGGGGGGGGGGG
XM_005245570.1:c.124+37_124+38insGGGGGGGGGGGGG	XP_005245627.1:n.124+37_124+38insGGGGGGGGGGGGG
XM_005245571.1:c.124+37_124+38insGGGGGGGGGGGGG	XP_005245628.1:n.124+37_124+38insGGGGGGGGGGGGG
XM_006711605.2:c.-93+578_-93+579insGGGGGGGGGGGGG	XP_006711668.1:n.-93+578_-93+579insGGGGGGGGGGGGG
XM_006711606.1:c.-93+606_-93+607insGGGGGGGGGGGGG	XP_006711669.1:n.-93+606_-93+607insGGGGGGGGGGGGG
XM_006711605.3:c.-93+578_-93+579insGGGGGGGGGGGGG	XP_006711668.1:n.-93+578_-93+579insGGGGGGGGGGGGG
XM_006711606.3:c.-93+606_-93+607insGGGGGGGGGGGGG	XP_006711669.1:n.-93+606_-93+607insGGGGGGGGGGGGG
XM_017002748.1:c.124+37_124+38insGGGGGGGGGGGGG	XP_016858237.1:n.124+37_124+38insGGGGGGGGGGGGG
XM_017002749.1:c.124+37_124+38insGGGGGGGGGGGGG	XP_016858238.1:n.124+37_124+38insGGGGGGGGGGGGG
XM_017002750.1:c.124+37_124+38insGGGGGGGGGGGGG	XP_016858239.1:n.124+37_124+38insGGGGGGGGGGGGG
NM_003929.3:c.124+37_124+38insGGGGGGGGGGGGG MANE Select	NP_003920.1:n.124+37_124+38insGGGGGGGGGGGGG
NM_001135662.2:c.124+37_124+38insGGGGGGGGGGGGG	NP_001129134.1:n.124+37_124+38insGGGGGGGGGGGGG
NM_001135663.2:c.124+37_124+38insGGGGGGGGGGGGG	NP_001129135.1:n.124+37_124+38insGGGGGGGGGGGGG
NM_001135664.2:c.-93+477_-93+478insGGGGGGGGGGGGG	NP_001129136.1:n.-93+477_-93+478insGGGGGGGGGGGGG