Canonical Allele Identifier: CA1168017611

Gene: USP24

Linked Data

• dbSNP Id: rs1165226

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55142332C>A , CM000663.2:g.55142332C>A	GRCh38
NC_000001.10:g.55608005C>A , CM000663.1:g.55608005C>A	GRCh37
NC_000001.9:g.55380593C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000484447.6:c.2634+410G>T	ENSP00000489026.2:n.2634+410G>T
ENST00000294383.7:c.2634+410G>T MANE Select	ENSP00000294383.5:n.2634+410G>T
ENST00000294383.6:c.2634+410G>T	ENSP00000294383.5:n.2634+410G>T
NM_015306.2:c.2634+410G>T	NP_056121.2:n.2634+410G>T
XM_005270690.2:c.849+410G>T	XP_005270747.1:n.849+410G>T
XM_006710511.2:c.2631+410G>T	XP_006710574.2:n.2631+410G>T
XM_011541122.1:c.2634+410G>T	XP_011539424.1:n.2634+410G>T
XM_011541123.1:c.2634+410G>T	XP_011539425.1:n.2634+410G>T
XM_011541124.1:c.2634+410G>T	XP_011539426.1:n.2634+410G>T
XM_011541125.1:c.2634+410G>T	XP_011539427.1:n.2634+410G>T
XM_011541126.1:c.2634+410G>T	XP_011539428.1:n.2634+410G>T
XM_011541127.1:c.2634+410G>T	XP_011539429.1:n.2634+410G>T
XR_946595.1:n.2888+410G>T
XM_005270690.3:c.849+410G>T	XP_005270747.1:n.849+410G>T
XM_017000831.1:c.2694+410G>T	XP_016856320.1:n.2694+410G>T
XM_017000832.1:c.2691+410G>T	XP_016856321.1:n.2691+410G>T
XM_017000833.1:c.2169+410G>T	XP_016856322.1:n.2169+410G>T
XM_017000834.1:c.2109+410G>T	XP_016856323.1:n.2109+410G>T
XM_017000835.1:c.2694+410G>T	XP_016856324.1:n.2694+410G>T
XM_017000836.1:c.2694+410G>T	XP_016856325.1:n.2694+410G>T
XM_017000837.1:c.2694+410G>T	XP_016856326.1:n.2694+410G>T
XR_001737080.1:n.2952+410G>T
XR_001737081.1:n.2955+410G>T
XR_001737082.1:n.2955+410G>T
XR_001737083.1:n.2955+410G>T
NM_015306.3:c.2634+410G>T MANE Select	NP_056121.2:n.2634+410G>T