Canonical Allele Identifier: CA2650150588

Gene: RAB29

Linked Data

• gnomAD v4: 1-205775234-GCCGAGAAACTGGACCAGGCGCCGCGGAACCTCACCCACCGGGACTTCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775240_205775288del , CM000663.2:g.205775240_205775288del	GRCh38
NC_000001.10:g.205744368_205744416del , CM000663.1:g.205744368_205744416del	GRCh37
NC_000001.9:g.204010991_204011039del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-141_-131+38del
ENST00000235932.8:c.-131+91_-131+139del	ENSP00000235932.4:n.-131+91_-131+139del
ENST00000367139.7:c.-141_-131+38del
ENST00000414729.1:c.-327_-279del	ENSP00000402910.1:n.-327_-279del
ENST00000437324.6:c.-103_-93+38del
ENST00000468887.1:n.158_168+38del
ENST00000528078.1:c.-141_-131+38del
NM_001135662.1:c.-131+91_-131+139del	NP_001129134.1:n.-131+91_-131+139del
NM_001135663.1:c.-327_-279del	NP_001129135.1:n.-327_-279del
NM_001135664.1:c.-103_-93+38del
NM_003929.2:c.-141_-131+38del
XM_005245569.1:c.-136+91_-136+139del	XP_005245626.1:n.-136+91_-136+139del
XM_005245570.1:c.-146_-136+38del
XM_005245571.1:c.-131+119_-130-149del	XP_005245628.1:n.-131+119_-130-149del
XM_006711605.2:c.-93+91_-93+139del	XP_006711668.1:n.-93+91_-93+139del
XM_006711606.1:c.-93+119_-93+167del	XP_006711669.1:n.-93+119_-93+167del
XM_006711605.3:c.-93+91_-93+139del	XP_006711668.1:n.-93+91_-93+139del
XM_006711606.3:c.-93+119_-93+167del	XP_006711669.1:n.-93+119_-93+167del
XM_017002748.1:c.-141_-131+38del
XM_017002749.1:c.-146_-136+38del
XM_017002750.1:c.-131+91_-131+139del	XP_016858239.1:n.-131+91_-131+139del
NM_003929.3:c.-141_-131+38del
NM_001135662.2:c.-131+91_-131+139del	NP_001129134.1:n.-131+91_-131+139del
NM_001135663.2:c.-327_-279del	NP_001129135.1:n.-327_-279del
NM_001135664.2:c.-103_-93+38del