Canonical Allele Identifier: CA1559205601

Gene: RPS23 ATG10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82276483C= , CM000667.2:g.82276483C=	GRCh38
NC_000005.9:g.81572302C= , CM000667.1:g.81572302C=	GRCh37
NC_000005.8:g.81608058C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296674.13:c.200G= (RPS23) MANE Select	ENSP00000296674.8:p.Arg67=
ENST00000651545.1:c.200G= (RPS23)	ENSP00000498621.1:p.Arg67=
ENST00000296674.12:c.200G= (RPS23)	ENSP00000296674.8:p.Arg67=
ENST00000503605.1:n.409G= (RPS23)
ENST00000504293.5:n.295G= (RPS23)
ENST00000507980.1:c.200G= (RPS23)	ENSP00000422071.1:p.Arg67=
ENST00000510019.5:c.200G= (RPS23)	ENSP00000425833.1:p.Arg67=
ENST00000510210.5:c.200G= (RPS23)	ENSP00000427043.1:p.Arg67=
ENST00000512493.5:c.200G= (RPS23)	ENSP00000425865.1:p.Arg67=
ENST00000514253.2:n.530C= (ATG10)
NM_001025.4:c.200G= (RPS23)	NP_001016.1:p.Arg67=
NM_001025.5:c.200G= (RPS23) MANE Select	NP_001016.1:p.Arg67=