Canonical Allele Identifier: CA2754687478
Gene: USP40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233513385_233513386insTGT , CM000664.2:g.233513385_233513386insTGT GRCh38
NC_000002.11:g.234422031_234422032insTGT , CM000664.1:g.234422031_234422032insTGT GRCh37
NC_000002.10:g.234086770_234086771insTGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000678225.2:c.2384-764_2384-763insACA MANE Select ENSP00000502952.1:n.2384-764_2384-763insACA
ENST00000678225.1:c.2382-762_2382-761insACA ENSP00000502952.1:n.2382-762_2382-761insACA
ENST00000251722.10:c.2381-764_2381-763insACA ENSP00000251722.6:n.2381-764_2381-763insACA
ENST00000427112.6:c.2381-764_2381-763insACA ENSP00000387898.2:n.2381-764_2381-763insACA
ENST00000450966.5:c.2417-764_2417-763insACA ENSP00000415434.1:n.2417-764_2417-763insACA
NM_018218.2:c.2417-764_2417-763insACA NP_060688.1:n.2417-764_2417-763insACA
XM_006712612.2:c.2420-764_2420-763insACA XP_006712675.1:n.2420-764_2420-763insACA
XM_011511396.1:c.2420-764_2420-763insACA XP_011509698.1:n.2420-764_2420-763insACA
XM_011511397.1:c.2384-764_2384-763insACA XP_011509699.1:n.2384-764_2384-763insACA
XM_011511398.1:c.2420-764_2420-763insACA XP_011509700.1:n.2420-764_2420-763insACA
XM_011511399.1:c.2111-764_2111-763insACA XP_011509701.1:n.2111-764_2111-763insACA
XM_011511400.1:c.2000-764_2000-763insACA XP_011509702.1:n.2000-764_2000-763insACA
XM_011511401.1:c.2420-707_2420-706insACA XP_011509703.1:n.2420-707_2420-706insACA
XM_011511402.1:c.866-764_866-763insACA XP_011509704.1:n.866-764_866-763insACA
NM_001365479.1:c.2384-764_2384-763insACA NP_001352408.1:n.2384-764_2384-763insACA
NM_018218.3:c.2381-764_2381-763insACA NP_060688.2:n.2381-764_2381-763insACA
XM_006712612.3:c.2420-764_2420-763insACA XP_006712675.1:n.2420-764_2420-763insACA
XM_011511396.2:c.2420-764_2420-763insACA XP_011509698.1:n.2420-764_2420-763insACA
XM_011511397.2:c.2384-764_2384-763insACA XP_011509699.1:n.2384-764_2384-763insACA
XM_011511398.3:c.2420-764_2420-763insACA XP_011509700.1:n.2420-764_2420-763insACA
XM_011511399.2:c.2111-764_2111-763insACA XP_011509701.1:n.2111-764_2111-763insACA
XM_011511400.2:c.2000-764_2000-763insACA XP_011509702.1:n.2000-764_2000-763insACA
XM_011511401.2:c.2420-707_2420-706insACA XP_011509703.1:n.2420-707_2420-706insACA
XM_017004427.1:c.1349-764_1349-763insACA XP_016859916.1:n.1349-764_1349-763insACA
XM_017004428.1:c.866-764_866-763insACA XP_016859917.1:n.866-764_866-763insACA
XR_001738818.1:n.2435-764_2435-763insACA
XR_001738819.1:n.2435-764_2435-763insACA
XR_001738820.1:n.2509-764_2509-763insACA
NM_001365479.2:c.2384-764_2384-763insACA MANE Select NP_001352408.1:n.2384-764_2384-763insACA
NM_001382295.1:c.2384-764_2384-763insACA NP_001369224.1:n.2384-764_2384-763insACA
NM_001382296.1:c.2384-764_2384-763insACA NP_001369225.1:n.2384-764_2384-763insACA
NM_001382297.1:c.2384-764_2384-763insACA NP_001369226.1:n.2384-764_2384-763insACA
NM_001382298.1:c.2111-764_2111-763insACA NP_001369227.1:n.2111-764_2111-763insACA
NM_001382299.1:c.2228-764_2228-763insACA NP_001369228.1:n.2228-764_2228-763insACA
NM_001382300.1:c.2384-764_2384-763insACA NP_001369229.1:n.2384-764_2384-763insACA
NM_001382301.1:c.2384-764_2384-763insACA NP_001369230.1:n.2384-764_2384-763insACA
NM_018218.4:c.2381-764_2381-763insACA NP_060688.2:n.2381-764_2381-763insACA
NR_168049.1:n.2570-764_2570-763insACA
NR_168050.1:n.2568-764_2568-763insACA
NR_168051.1:n.2502-764_2502-763insACA
NR_168052.1:n.2502-764_2502-763insACA
NR_168053.1:n.2511-764_2511-763insACA
NR_168054.1:n.2323-764_2323-763insACA