Canonical Allele Identifier: CA2674480841

Gene: RPS23 ATG10

Linked Data

• gnomAD v4: 5-82276677-CTTAATTTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.82276681_82276689del , CM000667.2:g.82276681_82276689del	GRCh38
NC_000005.9:g.81572500_81572508del , CM000667.1:g.81572500_81572508del	GRCh37
NC_000005.8:g.81608256_81608264del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296674.13:c.165-168_165-160del (RPS23) MANE Select	ENSP00000296674.8:n.165-168_165-160del
ENST00000651545.1:c.165-168_165-160del (RPS23)	ENSP00000498621.1:n.165-168_165-160del
ENST00000296674.12:c.165-168_165-160del (RPS23)	ENSP00000296674.8:n.165-168_165-160del
ENST00000503605.1:n.374-168_374-160del (RPS23)
ENST00000504293.5:n.260-168_260-160del (RPS23)
ENST00000507980.1:c.165-168_165-160del (RPS23)	ENSP00000422071.1:n.165-168_165-160del
ENST00000510019.5:c.165-168_165-160del (RPS23)	ENSP00000425833.1:n.165-168_165-160del
ENST00000510210.5:c.165-168_165-160del (RPS23)	ENSP00000427043.1:n.165-168_165-160del
ENST00000512493.5:c.165-168_165-160del (RPS23)	ENSP00000425865.1:n.165-168_165-160del
ENST00000514253.2:n.728_736del (ATG10)
NM_001025.4:c.165-168_165-160del (RPS23)	NP_001016.1:n.165-168_165-160del
NM_001025.5:c.165-168_165-160del (RPS23) MANE Select	NP_001016.1:n.165-168_165-160del