Canonical Allele Identifier: CA3873929

Gene: RAB23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57210327T>C , CM000668.2:g.57210327T>C	GRCh38
NC_000006.11:g.57075125T>C , CM000668.1:g.57075125T>C	GRCh37
NC_000006.10:g.57183084T>C	NCBI36
NG_012170.1:g.16954A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016277.5:c.54A>G MANE Select	NP_057361.3:p.Gly18=
ENST00000468148.6:c.54A>G MANE Select	ENSP00000417610.1:p.Gly18=
NM_001278666.1:c.54A>G	NP_001265595.1:p.Gly18=
NM_001278666.2:c.54A>G	NP_001265595.1:p.Gly18=
NM_001278667.1:c.54A>G	NP_001265596.1:p.Gly18=
NM_001278667.2:c.54A>G	NP_001265596.1:p.Gly18=
NM_001278668.1:c.54A>G	NP_001265597.1:p.Gly18=
NM_001278668.2:c.54A>G	NP_001265597.1:p.Gly18=
NM_016277.4:c.54A>G	NP_057361.3:p.Gly18=
NM_183227.2:c.54A>G	NP_899050.1:p.Gly18=
NM_183227.3:c.54A>G	NP_899050.1:p.Gly18=
NR_103822.1:n.239A>G
NR_103822.2:n.232A>G
ENST00000317483.4:c.54A>G	ENSP00000320413.3:p.Gly18=
ENST00000468148.5:c.54A>G	ENSP00000417610.1:p.Gly18=
XM_005249179.2:c.54A>G	XP_005249236.1:p.Gly18=