Canonical Allele Identifier: CA10672639
Gene: USP24 HGNC NCBI

Linked Data

dbSNP Id: rs287235

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55212826G>C , CM000663.2:g.55212826G>C GRCh38
NC_000001.10:g.55678499G>C , CM000663.1:g.55678499G>C GRCh37
NC_000001.9:g.55451087G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000294383.7:c.324+1964C>G MANE Select ENSP00000294383.5:n.324+1964C>G
ENST00000294383.6:n.324+1964C>G ENSP00000294383.5:n.324+1964C>G
NM_015306.2:c.324+1964C>G NP_056121.2:n.324+1964C>G
XM_006710511.2:c.324+1964C>G XP_006710574.2:n.324+1964C>G
XM_011541122.1:c.324+1964C>G XP_011539424.1:n.324+1964C>G
XM_011541123.1:c.324+1964C>G XP_011539425.1:n.324+1964C>G
XM_011541124.1:c.324+1964C>G XP_011539426.1:n.324+1964C>G
XM_011541125.1:c.324+1964C>G XP_011539427.1:n.324+1964C>G
XM_011541126.1:c.324+1964C>G XP_011539428.1:n.324+1964C>G
XM_011541127.1:c.324+1964C>G XP_011539429.1:n.324+1964C>G
XR_946595.1:n.578+1964C>G
XM_017000831.1:c.324+1964C>G XP_016856320.1:n.324+1964C>G
XM_017000832.1:c.324+1964C>G XP_016856321.1:n.324+1964C>G
XM_017000833.1:c.-202+1780C>G XP_016856322.1:n.-202+1780C>G
XM_017000834.1:c.-202+1780C>G XP_016856323.1:n.-202+1780C>G
XM_017000835.1:c.324+1964C>G XP_016856324.1:n.324+1964C>G
XM_017000836.1:c.324+1964C>G XP_016856325.1:n.324+1964C>G
XM_017000837.1:c.324+1964C>G XP_016856326.1:n.324+1964C>G
XR_001737080.1:n.582+1964C>G
XR_001737081.1:n.585+1964C>G
XR_001737082.1:n.585+1964C>G
XR_001737083.1:n.585+1964C>G
NM_015306.3:c.324+1964C>G MANE Select NP_056121.2:n.324+1964C>G