Canonical Allele Identifier: CA2482718100

Gene: RAB29

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775262_205775263delinsAC , CM000663.2:g.205775262_205775263delinsAC	GRCh38
NC_000001.10:g.205744390_205744391delinsAC , CM000663.1:g.205744390_205744391delinsAC	GRCh37
NC_000001.9:g.204011013_204011014delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-131+10_-131+11delinsGT MANE Select	ENSP00000356107.3:n.-131+10_-131+11delinsGT
ENST00000235932.8:c.-131+111_-131+112delinsGT	ENSP00000235932.4:n.-131+111_-131+112delinsGT
ENST00000367139.7:c.-131+10_-131+11delinsGT	ENSP00000356107.3:n.-131+10_-131+11delinsGT
ENST00000414729.1:c.-307_-306delinsGT	ENSP00000402910.1:n.-307_-306delinsGT
ENST00000437324.6:c.-93+10_-93+11delinsGT	ENSP00000416613.2:n.-93+10_-93+11delinsGT
ENST00000468887.1:n.168+10_168+11delinsGT
ENST00000528078.1:c.-131+10_-131+11delinsGT	ENSP00000431483.1:n.-131+10_-131+11delinsGT
NM_001135662.1:c.-131+111_-131+112delinsGT	NP_001129134.1:n.-131+111_-131+112delinsGT
NM_001135663.1:c.-307_-306delinsGT	NP_001129135.1:n.-307_-306delinsGT
NM_001135664.1:c.-93+10_-93+11delinsGT	NP_001129136.1:n.-93+10_-93+11delinsGT
NM_003929.2:c.-131+10_-131+11delinsGT	NP_003920.1:n.-131+10_-131+11delinsGT
XM_005245569.1:c.-136+111_-136+112delinsGT	XP_005245626.1:n.-136+111_-136+112delinsGT
XM_005245570.1:c.-136+10_-136+11delinsGT	XP_005245627.1:n.-136+10_-136+11delinsGT
XM_005245571.1:c.-131+139_-131+140delinsGT	XP_005245628.1:n.-131+139_-131+140delinsGT
XM_006711605.2:c.-93+111_-93+112delinsGT	XP_006711668.1:n.-93+111_-93+112delinsGT
XM_006711606.1:c.-93+139_-93+140delinsGT	XP_006711669.1:n.-93+139_-93+140delinsGT
XM_006711605.3:c.-93+111_-93+112delinsGT	XP_006711668.1:n.-93+111_-93+112delinsGT
XM_006711606.3:c.-93+139_-93+140delinsGT	XP_006711669.1:n.-93+139_-93+140delinsGT
XM_017002748.1:c.-131+10_-131+11delinsGT	XP_016858237.1:n.-131+10_-131+11delinsGT
XM_017002749.1:c.-136+10_-136+11delinsGT	XP_016858238.1:n.-136+10_-136+11delinsGT
XM_017002750.1:c.-131+111_-131+112delinsGT	XP_016858239.1:n.-131+111_-131+112delinsGT
NM_003929.3:c.-131+10_-131+11delinsGT MANE Select	NP_003920.1:n.-131+10_-131+11delinsGT
NM_001135662.2:c.-131+111_-131+112delinsGT	NP_001129134.1:n.-131+111_-131+112delinsGT
NM_001135663.2:c.-307_-306delinsGT	NP_001129135.1:n.-307_-306delinsGT
NM_001135664.2:c.-93+10_-93+11delinsGT	NP_001129136.1:n.-93+10_-93+11delinsGT