Canonical Allele Identifier: CA1630426192

Gene: RAB23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57194681G= , CM000668.2:g.57194681G=	GRCh38
NC_000006.11:g.57059479G= , CM000668.1:g.57059479G=	GRCh37
NC_000006.10:g.57167438G=	NCBI36
NG_012170.1:g.32600C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000468148.6:c.481+89C= MANE Select	ENSP00000417610.1:n.481+89C=
ENST00000317483.4:c.481+89C=	ENSP00000320413.3:n.481+89C=
ENST00000468148.5:c.481+89C=	ENSP00000417610.1:n.481+89C=
NM_001278666.1:c.481+89C=	NP_001265595.1:n.481+89C=
NM_001278667.1:c.481+89C=	NP_001265596.1:n.481+89C=
NM_001278668.1:c.481+89C=	NP_001265597.1:n.481+89C=
NM_016277.4:c.481+89C=	NP_057361.3:n.481+89C=
NM_183227.2:c.481+89C=	NP_899050.1:n.481+89C=
NR_103822.1:n.341-747C=
XM_005249179.2:c.399-747C=	XP_005249236.1:n.399-747C=
NM_016277.5:c.481+89C= MANE Select	NP_057361.3:n.481+89C=
NM_001278666.2:c.481+89C=	NP_001265595.1:n.481+89C=
NM_001278667.2:c.481+89C=	NP_001265596.1:n.481+89C=
NM_001278668.2:c.481+89C=	NP_001265597.1:n.481+89C=
NM_183227.3:c.481+89C=	NP_899050.1:n.481+89C=
NR_103822.2:n.334-747C=