Canonical Allele Identifier: CA2482718139

Gene: RAB29

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205775337G= , CM000663.2:g.205775337G=	GRCh38
NC_000001.10:g.205744465G= , CM000663.1:g.205744465G=	GRCh37
NC_000001.9:g.204011088G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367139.8:c.-195C= MANE Select	ENSP00000356107.3:n.-195C=
ENST00000235932.8:c.-131+37C=	ENSP00000235932.4:n.-131+37C=
ENST00000367139.7:c.-195C=	ENSP00000356107.3:n.-195C=
ENST00000414729.1:c.-381C=	ENSP00000402910.1:n.-381C=
ENST00000437324.6:c.-157C=	ENSP00000416613.2:n.-157C=
ENST00000468887.1:n.104C=
ENST00000528078.1:c.-195C=	ENSP00000431483.1:n.-195C=
NM_001135662.1:c.-131+37C=	NP_001129134.1:n.-131+37C=
NM_001135663.1:c.-381C=	NP_001129135.1:n.-381C=
NM_001135664.1:c.-157C=	NP_001129136.1:n.-157C=
NM_003929.2:c.-195C=	NP_003920.1:n.-195C=
XM_005245569.1:c.-136+37C=	XP_005245626.1:n.-136+37C=
XM_005245570.1:c.-200C=	XP_005245627.1:n.-200C=
XM_005245571.1:c.-131+65C=	XP_005245628.1:n.-131+65C=
XM_006711605.2:c.-93+37C=	XP_006711668.1:n.-93+37C=
XM_006711606.1:c.-93+65C=	XP_006711669.1:n.-93+65C=
XM_006711605.3:c.-93+37C=	XP_006711668.1:n.-93+37C=
XM_006711606.3:c.-93+65C=	XP_006711669.1:n.-93+65C=
XM_017002748.1:c.-195C=	XP_016858237.1:n.-195C=
XM_017002749.1:c.-200C=	XP_016858238.1:n.-200C=
XM_017002750.1:c.-131+37C=	XP_016858239.1:n.-131+37C=
NM_003929.3:c.-195C= MANE Select	NP_003920.1:n.-195C=
NM_001135662.2:c.-131+37C=	NP_001129134.1:n.-131+37C=
NM_001135663.2:c.-381C=	NP_001129135.1:n.-381C=
NM_001135664.2:c.-157C=	NP_001129136.1:n.-157C=