Canonical Allele Identifier: CA445238000
Gene: RPS23 HGNC NCBI
ATG10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.81572208A>T (hg19)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000296674.13:c.285+9T>A (RPS23) MANE Select ENSP00000296674.8:n.285+9T>A
ENST00000651545.1:c.285+9T>A (RPS23) ENSP00000498621.1:n.285+9T>A
ENST00000296674.12:c.285+9T>A (RPS23) ENSP00000296674.8:n.285+9T>A
ENST00000503605.1:n.494+9T>A (RPS23)
ENST00000504293.5:n.380+9T>A (RPS23)
ENST00000507980.1:c.294T>A (RPS23) ENSP00000422071.1:p.Ile98=
ENST00000510019.5:c.232+62T>A (RPS23) ENSP00000425833.1:n.232+62T>A
ENST00000510210.5:c.285+9T>A (RPS23) ENSP00000427043.1:n.285+9T>A
ENST00000512493.5:c.285+9T>A (RPS23) ENSP00000425865.1:n.285+9T>A
ENST00000514253.2:n.436A>T (ATG10)
NM_001025.4:c.285+9T>A (RPS23) NP_001016.1:n.285+9T>A
NM_001025.5:c.285+9T>A (RPS23) MANE Select NP_001016.1:n.285+9T>A
Search 100 bp 5'
Search 100 bp 3'