Canonical Allele Identifier: CA445237998

Gene: RPS23 ATG10

Linked Data

• MyVariant Identifiers: chr5:g.81572208A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82276389A>G , CM000667.2:g.82276389A>G	GRCh38
NC_000005.9:g.81572208A>G , CM000667.1:g.81572208A>G	GRCh37
NC_000005.8:g.81607964A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296674.13:c.285+9T>C (RPS23) MANE Select	ENSP00000296674.8:n.285+9T>C
ENST00000651545.1:c.285+9T>C (RPS23)	ENSP00000498621.1:n.285+9T>C
ENST00000296674.12:c.285+9T>C (RPS23)	ENSP00000296674.8:n.285+9T>C
ENST00000503605.1:n.494+9T>C (RPS23)
ENST00000504293.5:n.380+9T>C (RPS23)
ENST00000507980.1:c.294T>C (RPS23)	ENSP00000422071.1:p.Ile98=
ENST00000510019.5:c.232+62T>C (RPS23)	ENSP00000425833.1:n.232+62T>C
ENST00000510210.5:c.285+9T>C (RPS23)	ENSP00000427043.1:n.285+9T>C
ENST00000512493.5:c.285+9T>C (RPS23)	ENSP00000425865.1:n.285+9T>C
ENST00000514253.2:n.436A>G (ATG10)
NM_001025.4:c.285+9T>C (RPS23)	NP_001016.1:n.285+9T>C
NM_001025.5:c.285+9T>C (RPS23) MANE Select	NP_001016.1:n.285+9T>C