Canonical Allele Identifier: CA2482718140

Gene: RAB29

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775339_205775352delinsCCAGATGATGGGGA , CM000663.2:g.205775339_205775352delinsCCAGATGATGGGGA	GRCh38
NC_000001.10:g.205744467_205744480delinsCCAGATGATGGGGA , CM000663.1:g.205744467_205744480delinsCCAGATGATGGGGA	GRCh37
NC_000001.9:g.204011090_204011103delinsCCAGATGATGGGGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-210_-197delinsTCCCCATCATCTGG MANE Select	ENSP00000356107.3:n.-210_-197delinsTCCCCATCATCTGG
ENST00000235932.8:c.-131+22_-131+35delinsTCCCCATCATCTGG	ENSP00000235932.4:n.-131+22_-131+35delinsTCCCCATCATCTGG
ENST00000367139.7:c.-210_-197delinsTCCCCATCATCTGG	ENSP00000356107.3:n.-210_-197delinsTCCCCATCATCTGG
ENST00000414729.1:c.-396_-383delinsTCCCCATCATCTGG	ENSP00000402910.1:n.-396_-383delinsTCCCCATCATCTGG
ENST00000437324.6:c.-172_-159delinsTCCCCATCATCTGG	ENSP00000416613.2:n.-172_-159delinsTCCCCATCATCTGG
ENST00000468887.1:n.89_102delinsTCCCCATCATCTGG
ENST00000528078.1:c.-210_-197delinsTCCCCATCATCTGG	ENSP00000431483.1:n.-210_-197delinsTCCCCATCATCTGG
NM_001135662.1:c.-131+22_-131+35delinsTCCCCATCATCTGG	NP_001129134.1:n.-131+22_-131+35delinsTCCCCATCATCTGG
NM_001135663.1:c.-396_-383delinsTCCCCATCATCTGG	NP_001129135.1:n.-396_-383delinsTCCCCATCATCTGG
NM_001135664.1:c.-172_-159delinsTCCCCATCATCTGG	NP_001129136.1:n.-172_-159delinsTCCCCATCATCTGG
NM_003929.2:c.-210_-197delinsTCCCCATCATCTGG	NP_003920.1:n.-210_-197delinsTCCCCATCATCTGG
XM_005245569.1:c.-136+22_-136+35delinsTCCCCATCATCTGG	XP_005245626.1:n.-136+22_-136+35delinsTCCCCATCATCTGG
XM_005245570.1:c.-215_-202delinsTCCCCATCATCTGG	XP_005245627.1:n.-215_-202delinsTCCCCATCATCTGG
XM_005245571.1:c.-131+50_-131+63delinsTCCCCATCATCTGG	XP_005245628.1:n.-131+50_-131+63delinsTCCCCATCATCTGG
XM_006711605.2:c.-93+22_-93+35delinsTCCCCATCATCTGG	XP_006711668.1:n.-93+22_-93+35delinsTCCCCATCATCTGG
XM_006711606.1:c.-93+50_-93+63delinsTCCCCATCATCTGG	XP_006711669.1:n.-93+50_-93+63delinsTCCCCATCATCTGG
XM_006711605.3:c.-93+22_-93+35delinsTCCCCATCATCTGG	XP_006711668.1:n.-93+22_-93+35delinsTCCCCATCATCTGG
XM_006711606.3:c.-93+50_-93+63delinsTCCCCATCATCTGG	XP_006711669.1:n.-93+50_-93+63delinsTCCCCATCATCTGG
XM_017002748.1:c.-210_-197delinsTCCCCATCATCTGG	XP_016858237.1:n.-210_-197delinsTCCCCATCATCTGG
XM_017002749.1:c.-215_-202delinsTCCCCATCATCTGG	XP_016858238.1:n.-215_-202delinsTCCCCATCATCTGG
XM_017002750.1:c.-131+22_-131+35delinsTCCCCATCATCTGG	XP_016858239.1:n.-131+22_-131+35delinsTCCCCATCATCTGG
NM_003929.3:c.-210_-197delinsTCCCCATCATCTGG MANE Select	NP_003920.1:n.-210_-197delinsTCCCCATCATCTGG
NM_001135662.2:c.-131+22_-131+35delinsTCCCCATCATCTGG	NP_001129134.1:n.-131+22_-131+35delinsTCCCCATCATCTGG
NM_001135663.2:c.-396_-383delinsTCCCCATCATCTGG	NP_001129135.1:n.-396_-383delinsTCCCCATCATCTGG
NM_001135664.2:c.-172_-159delinsTCCCCATCATCTGG	NP_001129136.1:n.-172_-159delinsTCCCCATCATCTGG