Canonical Allele Identifier: CA360355822

Gene: RPS23 ATG10

Linked Data

• MyVariant Identifiers: chr5:g.81572227T>G (hg19) ; chr5:g.82276408T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82276408T>G , CM000667.2:g.82276408T>G	GRCh38
NC_000005.9:g.81572227T>G , CM000667.1:g.81572227T>G	GRCh37
NC_000005.8:g.81607983T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296674.13:c.275A>C (RPS23) MANE Select	ENSP00000296674.8:p.Asn92Thr
ENST00000651545.1:c.275A>C (RPS23)	ENSP00000498621.1:p.Asn92Thr
ENST00000296674.12:c.275A>C (RPS23)	ENSP00000296674.8:p.Asn92Thr
ENST00000503605.1:n.484A>C (RPS23)
ENST00000504293.5:n.370A>C (RPS23)
ENST00000507980.1:c.275A>C (RPS23)	ENSP00000422071.1:p.Asn92Thr
ENST00000510019.5:c.232+43A>C (RPS23)	ENSP00000425833.1:n.232+43A>C
ENST00000510210.5:c.275A>C (RPS23)	ENSP00000427043.1:p.Asn92Thr
ENST00000512493.5:c.275A>C (RPS23)	ENSP00000425865.1:p.Asn92Thr
ENST00000514253.2:n.455T>G (ATG10)
NM_001025.4:c.275A>C (RPS23)	NP_001016.1:p.Asn92Thr
NM_001025.5:c.275A>C (RPS23) MANE Select	NP_001016.1:p.Asn92Thr