Canonical Allele Identifier: CA2771180905
Gene: RAB23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.57189968del , CM000668.2:g.57189968del GRCh38
NC_000006.11:g.57054766del , CM000668.1:g.57054766del GRCh37
NC_000006.10:g.57162725del NCBI36
NG_012170.1:g.37313del

Transcript Alleles

HGVS Amino-acid Change
ENST00000468148.6:c.*493del MANE Select ENSP00000417610.1:n.*493del
ENST00000317483.4:c.*493del ENSP00000320413.3:n.*493del
ENST00000468148.5:c.*493del ENSP00000417610.1:n.*493del
NM_001278666.1:c.*493del NP_001265595.1:n.*493del
NM_001278667.1:c.*493del NP_001265596.1:n.*493del
NM_001278668.1:c.*493del NP_001265597.1:n.*493del
NM_016277.4:c.*493del NP_057361.3:n.*493del
NM_183227.2:c.*493del NP_899050.1:n.*493del
NR_103822.1:n.1066del
NM_016277.5:c.*493del MANE Select NP_057361.3:n.*493del
NM_001278666.2:c.*493del NP_001265595.1:n.*493del
NM_001278667.2:c.*493del NP_001265596.1:n.*493del
NM_001278668.2:c.*493del NP_001265597.1:n.*493del
NM_183227.3:c.*493del NP_899050.1:n.*493del
NR_103822.2:n.1059del