Canonical Allele Identifier: CA1630424611
Gene: RAB23 HGNC NCBI

Linked Data

dbSNP Id: rs1764807868

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.57190667del , CM000668.2:g.57190667del GRCh38
NC_000006.11:g.57055465del , CM000668.1:g.57055465del GRCh37
NC_000006.10:g.57163424del NCBI36
NG_012170.1:g.36614del

Transcript Alleles

HGVS Amino-acid Change
ENST00000468148.6:c.575-67del MANE Select ENSP00000417610.1:n.575-67del
ENST00000317483.4:c.575-67del ENSP00000320413.3:n.575-67del
ENST00000468148.5:c.575-67del ENSP00000417610.1:n.575-67del
NM_001278666.1:c.575-67del NP_001265595.1:n.575-67del
NM_001278667.1:c.575-67del NP_001265596.1:n.575-67del
NM_001278668.1:c.575-67del NP_001265597.1:n.575-67del
NM_016277.4:c.575-67del NP_057361.3:n.575-67del
NM_183227.2:c.575-67del NP_899050.1:n.575-67del
NR_103822.1:n.434-67del
NM_016277.5:c.575-67del MANE Select NP_057361.3:n.575-67del
NM_001278666.2:c.575-67del NP_001265595.1:n.575-67del
NM_001278667.2:c.575-67del NP_001265596.1:n.575-67del
NM_001278668.2:c.575-67del NP_001265597.1:n.575-67del
NM_183227.3:c.575-67del NP_899050.1:n.575-67del
NR_103822.2:n.427-67del