Canonical Allele Identifier: CA1630424560
Gene: RAB23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.57190572G= , CM000668.2:g.57190572G= GRCh38
NC_000006.11:g.57055370G= , CM000668.1:g.57055370G= GRCh37
NC_000006.10:g.57163329G= NCBI36
NG_012170.1:g.36709C=

Transcript Alleles

HGVS Amino-acid change
ENST00000468148.6:c.603C= MANE Select ENSP00000417610.1:p.His201=
ENST00000317483.4:c.603C= ENSP00000320413.3:p.His201=
ENST00000468148.5:c.603C= ENSP00000417610.1:p.His201=
NM_001278666.1:c.603C= NP_001265595.1:p.His201=
NM_001278667.1:c.603C= NP_001265596.1:p.His201=
NM_001278668.1:c.603C= NP_001265597.1:p.His201=
NM_016277.4:c.603C= NP_057361.3:p.His201=
NM_183227.2:c.603C= NP_899050.1:p.His201=
NR_103822.1:n.462C=
NM_016277.5:c.603C= MANE Select NP_057361.3:p.His201=
NM_001278666.2:c.603C= NP_001265595.1:p.His201=
NM_001278667.2:c.603C= NP_001265596.1:p.His201=
NM_001278668.2:c.603C= NP_001265597.1:p.His201=
NM_183227.3:c.603C= NP_899050.1:p.His201=
NR_103822.2:n.455C=