Canonical Allele Identifier: CA1630424024

Gene: RAB23 BAG2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57189409A= , CM000668.2:g.57189409A=	GRCh38
NC_000006.11:g.57054207A= , CM000668.1:g.57054207A=	GRCh37
NC_000006.10:g.57162166A=	NCBI36
NG_012170.1:g.37872T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468148.6:c.*1052T= (RAB23) MANE Select	ENSP00000417610.1:n.*1052T=
ENST00000317483.4:c.*1052T= (RAB23)	ENSP00000320413.3:n.*1052T=
ENST00000370693.5:c.*5219A= (BAG2) MANE Select	ENSP00000359727.4:n.*5219A=
ENST00000468148.5:c.*1052T= (RAB23)	ENSP00000417610.1:n.*1052T=
NM_001278666.1:c.*1052T= (RAB23)	NP_001265595.1:n.*1052T=
NM_001278667.1:c.*1052T= (RAB23)	NP_001265596.1:n.*1052T=
NM_001278668.1:c.*1052T= (RAB23)	NP_001265597.1:n.*1052T=
NM_016277.4:c.*1052T= (RAB23)	NP_057361.3:n.*1052T=
NM_183227.2:c.*1052T= (RAB23)	NP_899050.1:n.*1052T=
NR_103822.1:n.1625T= (RAB23)
NM_004282.4:c.*5219A= (BAG2) MANE Select	NP_004273.1:n.*5219A=
NM_016277.5:c.*1052T= (RAB23) MANE Select	NP_057361.3:n.*1052T=
NM_001278666.2:c.*1052T= (RAB23)	NP_001265595.1:n.*1052T=
NM_001278667.2:c.*1052T= (RAB23)	NP_001265596.1:n.*1052T=
NM_001278668.2:c.*1052T= (RAB23)	NP_001265597.1:n.*1052T=
NM_183227.3:c.*1052T= (RAB23)	NP_899050.1:n.*1052T=
NR_103822.2:n.1618T= (RAB23)