Canonical Allele Identifier: CA2482718123

Gene: RAB29

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775299T= , CM000663.2:g.205775299T=	GRCh38
NC_000001.10:g.205744427T= , CM000663.1:g.205744427T=	GRCh37
NC_000001.9:g.204011050T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-157A= MANE Select	ENSP00000356107.3:n.-157A=
ENST00000235932.8:c.-131+75A=	ENSP00000235932.4:n.-131+75A=
ENST00000367139.7:c.-157A=	ENSP00000356107.3:n.-157A=
ENST00000414729.1:c.-343A=	ENSP00000402910.1:n.-343A=
ENST00000437324.6:c.-119A=	ENSP00000416613.2:n.-119A=
ENST00000468887.1:n.142A=
ENST00000528078.1:c.-157A=	ENSP00000431483.1:n.-157A=
NM_001135662.1:c.-131+75A=	NP_001129134.1:n.-131+75A=
NM_001135663.1:c.-343A=	NP_001129135.1:n.-343A=
NM_001135664.1:c.-119A=	NP_001129136.1:n.-119A=
NM_003929.2:c.-157A=	NP_003920.1:n.-157A=
XM_005245569.1:c.-136+75A=	XP_005245626.1:n.-136+75A=
XM_005245570.1:c.-162A=	XP_005245627.1:n.-162A=
XM_005245571.1:c.-131+103A=	XP_005245628.1:n.-131+103A=
XM_006711605.2:c.-93+75A=	XP_006711668.1:n.-93+75A=
XM_006711606.1:c.-93+103A=	XP_006711669.1:n.-93+103A=
XM_006711605.3:c.-93+75A=	XP_006711668.1:n.-93+75A=
XM_006711606.3:c.-93+103A=	XP_006711669.1:n.-93+103A=
XM_017002748.1:c.-157A=	XP_016858237.1:n.-157A=
XM_017002749.1:c.-162A=	XP_016858238.1:n.-162A=
XM_017002750.1:c.-131+75A=	XP_016858239.1:n.-131+75A=
NM_003929.3:c.-157A= MANE Select	NP_003920.1:n.-157A=
NM_001135662.2:c.-131+75A=	NP_001129134.1:n.-131+75A=
NM_001135663.2:c.-343A=	NP_001129135.1:n.-343A=
NM_001135664.2:c.-119A=	NP_001129136.1:n.-119A=