Canonical Allele Identifier: CA1357069

Gene: RAB29

Linked Data

• dbSNP Id: rs759299956
• ExAC: 1:205744089 A / AG
• gnomAD v2: 1-205744089-A-AG
• gnomAD v4: 1-205774961-A-AG
• MyVariant Identifiers: chr1:g.205744089_205744090insG (hg19) ; chr1:g.205774961_205774962insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205774962dup , CM000663.2:g.205774962dup	GRCh38
NC_000001.10:g.205744090dup , CM000663.1:g.205744090dup	GRCh37
NC_000001.9:g.204010713dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-6dup MANE Select	ENSP00000356107.3:n.-6dup
ENST00000235932.8:c.-6dup	ENSP00000235932.4:n.-6dup
ENST00000367139.7:c.-6dup	ENSP00000356107.3:n.-6dup
ENST00000414729.1:c.-6dup	ENSP00000402910.1:n.-6dup
ENST00000437324.6:c.-93+311dup	ENSP00000416613.2:n.-93+311dup
ENST00000446390.6:c.-6dup	ENSP00000389899.2:n.-6dup
ENST00000468887.1:n.168+311dup
ENST00000492534.1:n.190dup
ENST00000528078.1:c.-6dup	ENSP00000431483.1:n.-6dup
ENST00000533111.1:n.81+167dup
NM_001135662.1:c.-6dup	NP_001129134.1:n.-6dup
NM_001135663.1:c.-6dup	NP_001129135.1:n.-6dup
NM_001135664.1:c.-93+311dup	NP_001129136.1:n.-93+311dup
NM_003929.2:c.-6dup	NP_003920.1:n.-6dup
XM_005245569.1:c.-6dup	XP_005245626.1:n.-6dup
XM_005245570.1:c.-6dup	XP_005245627.1:n.-6dup
XM_005245571.1:c.-6dup	XP_005245628.1:n.-6dup
XM_006711605.2:c.-93+412dup	XP_006711668.1:n.-93+412dup
XM_006711606.1:c.-93+440dup	XP_006711669.1:n.-93+440dup
XM_006711605.3:c.-93+412dup	XP_006711668.1:n.-93+412dup
XM_006711606.3:c.-93+440dup	XP_006711669.1:n.-93+440dup
XM_017002748.1:c.-6dup	XP_016858237.1:n.-6dup
XM_017002749.1:c.-6dup	XP_016858238.1:n.-6dup
XM_017002750.1:c.-6dup	XP_016858239.1:n.-6dup
NM_003929.3:c.-6dup MANE Select	NP_003920.1:n.-6dup
NM_001135662.2:c.-6dup	NP_001129134.1:n.-6dup
NM_001135663.2:c.-6dup	NP_001129135.1:n.-6dup
NM_001135664.2:c.-93+311dup	NP_001129136.1:n.-93+311dup