Canonical Allele Identifier: CA1335778192
Gene: USP40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233513433_233513437delinsGACAA , CM000664.2:g.233513433_233513437delinsGACAA GRCh38
NC_000002.11:g.234422079_234422083delinsGACAA , CM000664.1:g.234422079_234422083delinsGACAA GRCh37
NC_000002.10:g.234086818_234086822delinsGACAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000678225.2:c.2384-815_2384-811delinsTTGTC MANE Select ENSP00000502952.1:n.2384-815_2384-811deli...
ENST00000678225.1:c.2382-813_2382-809delinsTTGTC ENSP00000502952.1:n.2382-813_2382-809deli...
ENST00000251722.10:c.2381-815_2381-811delinsTTGTC ENSP00000251722.6:n.2381-815_2381-811deli...
ENST00000427112.6:c.2381-815_2381-811delinsTTGTC ENSP00000387898.2:n.2381-815_2381-811deli...
ENST00000450966.5:c.2417-815_2417-811delinsTTGTC ENSP00000415434.1:n.2417-815_2417-811deli...
NM_018218.2:c.2417-815_2417-811delinsTTGTC NP_060688.1:n.2417-815_2417-811delinsTTGT...
XM_006712612.2:c.2420-815_2420-811delinsTTGTC XP_006712675.1:n.2420-815_2420-811delinsT...
XM_011511396.1:c.2420-815_2420-811delinsTTGTC XP_011509698.1:n.2420-815_2420-811delinsT...
XM_011511397.1:c.2384-815_2384-811delinsTTGTC XP_011509699.1:n.2384-815_2384-811delinsT...
XM_011511398.1:c.2420-815_2420-811delinsTTGTC XP_011509700.1:n.2420-815_2420-811delinsT...
XM_011511399.1:c.2111-815_2111-811delinsTTGTC XP_011509701.1:n.2111-815_2111-811delinsT...
XM_011511400.1:c.2000-815_2000-811delinsTTGTC XP_011509702.1:n.2000-815_2000-811delinsT...
XM_011511401.1:c.2420-758_2420-754delinsTTGTC XP_011509703.1:n.2420-758_2420-754delinsT...
XM_011511402.1:c.866-815_866-811delinsTTGTC XP_011509704.1:n.866-815_866-811delinsTTG...
NM_001365479.1:c.2384-815_2384-811delinsTTGTC NP_001352408.1:n.2384-815_2384-811delinsT...
NM_018218.3:c.2381-815_2381-811delinsTTGTC NP_060688.2:n.2381-815_2381-811delinsTTGT...
XM_006712612.3:c.2420-815_2420-811delinsTTGTC XP_006712675.1:n.2420-815_2420-811delinsT...
XM_011511396.2:c.2420-815_2420-811delinsTTGTC XP_011509698.1:n.2420-815_2420-811delinsT...
XM_011511397.2:c.2384-815_2384-811delinsTTGTC XP_011509699.1:n.2384-815_2384-811delinsT...
XM_011511398.3:c.2420-815_2420-811delinsTTGTC XP_011509700.1:n.2420-815_2420-811delinsT...
XM_011511399.2:c.2111-815_2111-811delinsTTGTC XP_011509701.1:n.2111-815_2111-811delinsT...
XM_011511400.2:c.2000-815_2000-811delinsTTGTC XP_011509702.1:n.2000-815_2000-811delinsT...
XM_011511401.2:c.2420-758_2420-754delinsTTGTC XP_011509703.1:n.2420-758_2420-754delinsT...
XM_017004427.1:c.1349-815_1349-811delinsTTGTC XP_016859916.1:n.1349-815_1349-811delinsT...
XM_017004428.1:c.866-815_866-811delinsTTGTC XP_016859917.1:n.866-815_866-811delinsTTG...
XR_001738818.1:n.2435-815_2435-811delinsTTGTC
XR_001738819.1:n.2435-815_2435-811delinsTTGTC
XR_001738820.1:n.2509-815_2509-811delinsTTGTC
NM_001365479.2:c.2384-815_2384-811delinsTTGTC MANE Select NP_001352408.1:n.2384-815_2384-811delinsT...
NM_001382295.1:c.2384-815_2384-811delinsTTGTC NP_001369224.1:n.2384-815_2384-811delinsT...
NM_001382296.1:c.2384-815_2384-811delinsTTGTC NP_001369225.1:n.2384-815_2384-811delinsT...
NM_001382297.1:c.2384-815_2384-811delinsTTGTC NP_001369226.1:n.2384-815_2384-811delinsT...
NM_001382298.1:c.2111-815_2111-811delinsTTGTC NP_001369227.1:n.2111-815_2111-811delinsT...
NM_001382299.1:c.2228-815_2228-811delinsTTGTC NP_001369228.1:n.2228-815_2228-811delinsT...
NM_001382300.1:c.2384-815_2384-811delinsTTGTC NP_001369229.1:n.2384-815_2384-811delinsT...
NM_001382301.1:c.2384-815_2384-811delinsTTGTC NP_001369230.1:n.2384-815_2384-811delinsT...
NM_018218.4:c.2381-815_2381-811delinsTTGTC NP_060688.2:n.2381-815_2381-811delinsTTGT...
NR_168049.1:n.2570-815_2570-811delinsTTGTC
NR_168050.1:n.2568-815_2568-811delinsTTGTC
NR_168051.1:n.2502-815_2502-811delinsTTGTC
NR_168052.1:n.2502-815_2502-811delinsTTGTC
NR_168053.1:n.2511-815_2511-811delinsTTGTC
NR_168054.1:n.2323-815_2323-811delinsTTGTC