Canonical Allele Identifier: CA1630424032

Linked Data

dbSNP Id: rs1736492364

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.57189415del , CM000668.2:g.57189415del GRCh38
NC_000006.11:g.57054213del , CM000668.1:g.57054213del GRCh37
NC_000006.10:g.57162172del NCBI36
NG_012170.1:g.37866del

Transcript Alleles

HGVS Amino-acid Change
ENST00000468148.6:c.*1046del (RAB23) MANE Select ENSP00000417610.1:n.*1046del
ENST00000317483.4:c.*1046del (RAB23) ENSP00000320413.3:n.*1046del
ENST00000370693.5:c.*5225del (BAG2) MANE Select ENSP00000359727.4:n.*5225del
ENST00000468148.5:c.*1046del (RAB23) ENSP00000417610.1:n.*1046del
NM_001278666.1:c.*1046del (RAB23) NP_001265595.1:n.*1046del
NM_001278667.1:c.*1046del (RAB23) NP_001265596.1:n.*1046del
NM_001278668.1:c.*1046del (RAB23) NP_001265597.1:n.*1046del
NM_016277.4:c.*1046del (RAB23) NP_057361.3:n.*1046del
NM_183227.2:c.*1046del (RAB23) NP_899050.1:n.*1046del
NR_103822.1:n.1619del (RAB23)
NM_004282.4:c.*5225del (BAG2) MANE Select NP_004273.1:n.*5225del
NM_016277.5:c.*1046del (RAB23) MANE Select NP_057361.3:n.*1046del
NM_001278666.2:c.*1046del (RAB23) NP_001265595.1:n.*1046del
NM_001278667.2:c.*1046del (RAB23) NP_001265596.1:n.*1046del
NM_001278668.2:c.*1046del (RAB23) NP_001265597.1:n.*1046del
NM_183227.3:c.*1046del (RAB23) NP_899050.1:n.*1046del
NR_103822.2:n.1612del (RAB23)