Canonical Allele Identifier: CA737009559
Gene: USP24 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55067069G>T , CM000663.2:g.55067069G>T GRCh38
NC_000001.10:g.55532742G>T , CM000663.1:g.55532742G>T GRCh37
NC_000001.9:g.55305330G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000294383.7:c.*1976C>A MANE Select ENSP00000294383.5:n.*1976C>A
ENST00000294383.6:c.9839C>A ENSP00000294383.5:n.9839C>A
NM_015306.2:c.*1976C>A NP_056121.2:n.*1976C>A
XM_005270690.2:c.*1976C>A XP_005270747.1:n.*1976C>A
XM_006710511.2:c.*1976C>A XP_006710574.2:n.*1976C>A
XM_011541122.1:c.*2080C>A XP_011539424.1:n.*2080C>A
XM_005270690.3:c.*1976C>A XP_005270747.1:n.*1976C>A
XM_017000831.1:c.*1976C>A XP_016856320.1:n.*1976C>A
XM_017000832.1:c.*1976C>A XP_016856321.1:n.*1976C>A
XM_017000833.1:c.*1976C>A XP_016856322.1:n.*1976C>A
XM_017000834.1:c.*1976C>A XP_016856323.1:n.*1976C>A
NM_015306.3:c.*1976C>A MANE Select NP_056121.2:n.*1976C>A
Search 100 bp 5'
Search 100 bp 3'