Canonical Allele Identifier: CA1630424557
Gene: RAB23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.57190567C= , CM000668.2:g.57190567C= GRCh38
NC_000006.11:g.57055365C= , CM000668.1:g.57055365C= GRCh37
NC_000006.10:g.57163324C= NCBI36
NG_012170.1:g.36714G=

Transcript Alleles

HGVS Amino-acid change
ENST00000468148.6:c.608G= MANE Select ENSP00000417610.1:p.Gly203=
ENST00000317483.4:c.608G= ENSP00000320413.3:p.Gly203=
ENST00000468148.5:c.608G= ENSP00000417610.1:p.Gly203=
NM_001278666.1:c.608G= NP_001265595.1:p.Gly203=
NM_001278667.1:c.608G= NP_001265596.1:p.Gly203=
NM_001278668.1:c.608G= NP_001265597.1:p.Gly203=
NM_016277.4:c.608G= NP_057361.3:p.Gly203=
NM_183227.2:c.608G= NP_899050.1:p.Gly203=
NR_103822.1:n.467G=
NM_016277.5:c.608G= MANE Select NP_057361.3:p.Gly203=
NM_001278666.2:c.608G= NP_001265595.1:p.Gly203=
NM_001278667.2:c.608G= NP_001265596.1:p.Gly203=
NM_001278668.2:c.608G= NP_001265597.1:p.Gly203=
NM_183227.3:c.608G= NP_899050.1:p.Gly203=
NR_103822.2:n.460G=