Canonical Allele Identifier: CA1139773944

Gene: USP24

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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