Canonical Allele Identifier: CA1011509701

Gene: RAB29

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205774797_205774798insCCCCCCCCCCC , CM000663.2:g.205774797_205774798insCCCCCCCCCCC	GRCh38
NC_000001.10:g.205743925_205743926insCCCCCCCCCCC , CM000663.1:g.205743925_205743926insCCCCCCCCCCC	GRCh37
NC_000001.9:g.204010548_204010549insCCCCCCCCCCC	NCBI36

Transcript Alleles

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