Canonical Allele Identifier: CA1630424381

Gene: RAB23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57190179C= , CM000668.2:g.57190179C=	GRCh38
NC_000006.11:g.57054977C= , CM000668.1:g.57054977C=	GRCh37
NC_000006.10:g.57162936C=	NCBI36
NG_012170.1:g.37102G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468148.6:c.*282G= MANE Select	ENSP00000417610.1:n.*282G=
ENST00000317483.4:c.*282G=	ENSP00000320413.3:n.*282G=
ENST00000468148.5:c.*282G=	ENSP00000417610.1:n.*282G=
NM_001278666.1:c.*282G=	NP_001265595.1:n.*282G=
NM_001278667.1:c.*282G=	NP_001265596.1:n.*282G=
NM_001278668.1:c.*282G=	NP_001265597.1:n.*282G=
NM_016277.4:c.*282G=	NP_057361.3:n.*282G=
NM_183227.2:c.*282G=	NP_899050.1:n.*282G=
NR_103822.1:n.855G=
NM_016277.5:c.*282G= MANE Select	NP_057361.3:n.*282G=
NM_001278666.2:c.*282G=	NP_001265595.1:n.*282G=
NM_001278667.2:c.*282G=	NP_001265596.1:n.*282G=
NM_001278668.2:c.*282G=	NP_001265597.1:n.*282G=
NM_183227.3:c.*282G=	NP_899050.1:n.*282G=
NR_103822.2:n.848G=